| 1 |
NCT02593396 |
Recruiting |
Bupropion in Sexual Dysfunction Among Methadone Maintenance Treatment Men |
- Sexual Dysfunctions, Psychological
- Hypoactive Sexual Desire Disorder
- Erectile Dysfunctions
|
- Drug: Bupropion hydrochloride sustained-release
- Drug: placebo
|
Interventional |
Phase 2 |
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Primary Purpose: Treatment
|
- Change from baseline in Clinical Global Impression Scale adapted for Sexual Function at (CGI-SF)-at 2,4,6.
- Change From Baseline in International Index of Erectile Function (IIEF) score at Weeks 2, 4 and 6
- Change from baseline in the individual domain scores: erectile function, orgasmic function, sexual desire, intercourse satisfaction and overall sexual satisfaction, of the IIEF at weeks 2, 4, 6
- Change from baseline in sexual desire inventory 2 (SDI2) score at weeks 2, 4,6,
|
70 |
Male |
18 Years to 65 Years (Adult) |
NCT02593396 |
AY001 |
|
August 2015 |
April 2018 |
August 2018 |
November 2, 2015 |
November 6, 2017 |
|
- University Malaya Medical Center
Kuala Lumpur, Selangor, Malaysia
|
| 2 |
NCT03087565 |
Recruiting |
Urinary and Sexual Functions After Subtotal Versus Total Abdominal Hysterectomy |
- Sexual Function Disturbances
- Urinary Function Disorders
|
- Procedure: subtotal hystrectomy
- Procedure: Total hystrectomy
|
Interventional |
Not Applicable |
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Filling cystometry
- Uroflowmetry
- Sexual functions
|
200 |
Female |
35 Years to 50 Years (Adult) |
NCT03087565 |
162 |
|
April 1, 2017 |
December 2017 |
December 2017 |
March 22, 2017 |
April 12, 2017 |
|
- Kasr Alainy medical school
Cairo, Egypt
|
| 3 |
NCT02859285 |
Recruiting |
A Study Evaluating the Effects of Topical Clitoral Estradiol Cream in Post Menopausal Women |
- Hypoactive Sexual Desire Disorder
|
- Other: Placebo vulvar cream
- Other: Estradiol vulvar cream
|
Interventional |
Not Applicable |
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Primary Purpose: Other
|
- 19 point validated Female Function Index.
- 36 point RAND health survey.
|
30 |
Female |
18 Years and older (Adult, Senior) |
NCT02859285 |
IRB # 15-18 |
|
April 2016 |
April 2018 |
December 31, 2018 |
August 9, 2016 |
September 21, 2017 |
|
- Waukesa Memorial Hospital
Waukesha, Wisconsin, United States
|
| 4 |
NCT03365518 |
Recruiting |
Innovations in the Treatment of Sexual Health Post Prostate Cancer Treatment: Comparing Mindfulness vs. CBT |
- Prostate Cancer
- Sexual Dysfunctions, Psychological
- Sexual Dysfunction, Physiological
- (and 3 more...)
|
- Behavioral: Cognitive Behavioural Therapy (CBT)
- Behavioral: Mindfulness-Based Therapy
|
Interventional |
Not Applicable |
- University of British Columbia
- Vancouver Prostate Centre
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Supportive Care
|
- Change in relationship satisfaction
- Change in sexual satisfaction/distress
- Change in sexual functioning (one of three different questionnaires depending on the participant's demographics)
- (and 4 more...)
|
141 |
All |
19 Years and older (Adult, Senior) |
NCT03365518 |
H17-02247
D2017-1893 |
INTROSPPECT |
December 2017 |
December 2018 |
June 2019 |
December 7, 2017 |
December 12, 2017 |
|
- Gordon & Leslie Diamond Health Centre -- Vancouver General Hospital
Vancouver, British Columbia, Canada
|
| 5 |
NCT03463707 |
Recruiting |
BP101 for Adults With Female Sexual Dysfunction |
- Hypoactive Sexual Desire Disorder
- Female Sexual Dysfunction
- Sexual Desire Disorder
|
|
Interventional |
Phase 3 |
|
Industry |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Primary Purpose: Treatment
|
- Satisfying sexual events
- Orgasms
- Female Sexual Function Index total score
- (and 11 more...)
|
256 |
Female |
21 Years to 50 Years (Adult) |
NCT03463707 |
BP101-SD02-RUS |
|
March 5, 2018 |
March 2019 |
July 2019 |
March 13, 2018 |
March 15, 2018 |
|
- V.M. Bekhterev Republic Clinical Psychiatric Hospital
Kazan', Russian Federation - N.A. Alexeev Moscow Psychiatric Clinical Hospital #1
Moscow, Russian Federation - Clinical Psychiatry Hospital №1
Nizhniy Novgorod, Russian Federation - (and 6 more...)
|
| 6 |
NCT03232801 |
Not yet recruiting |
A Mindfulness-based Intervention for Older Women With Low Sexual Desire |
- Hypoactive Sexual Desire Disorder
- Sexual Dysfunction
- Female Sexual Dysfunction
|
- Behavioral: mindfulness-based multicomponent intervention
- Behavioral: general health education group
|
Interventional |
Not Applicable |
- University of Pittsburgh
- National Institute on Aging (NIA)
- National Institutes of Health (NIH)
|
Other / NIH |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Single (Outcomes Assessor)
- Primary Purpose: Other
|
- Feasibility: Proportion of enrolled women participating in all sessions
- Acceptability: Proportion of women indicating "somewhat" or "very satisfied" on a 5-point Likert scale measure of intervention satisfaction
- Desire
|
50 |
Female |
50 Years and older (Adult, Senior) |
NCT03232801 |
PRO15060240 |
|
September 2018 |
September 2019 |
September 2019 |
July 28, 2017 |
July 28, 2017 |
|
|
| 7 |
NCT03189238 |
Recruiting |
Platelet Rich Plasma (PRP) Peri-urethral and Clitoral Injections for the Treatment of Female Orgasmic Disorder |
|
- Biological: Peri-urethral and clitoral injections
|
Interventional |
Phase 2 |
- Center for Vulvovaginal Disorders
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Double (Participant, Care Provider)
- Primary Purpose: Treatment
|
|
40 |
Female |
25 Years to 50 Years (Adult) |
NCT03189238 |
Pro00021800 |
PRP |
June 28, 2017 |
May 2019 |
July 2019 |
June 16, 2017 |
June 26, 2017 |
|
- The Center for Vulvovaginal Disorders
Washington, D.C., District of Columbia, United States
|
| 8 |
NCT02770768 |
Recruiting |
Effects of Flibanserin on the Pre- and Post-menopausal Female Brain |
- Hypoactive Sexual Desire Disorder
|
- Drug: Flibanserin
- Drug: Placebo
|
Interventional |
Not Applicable |
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Double (Participant, Investigator)
- Primary Purpose: Basic Science
|
- EEG Results: Evoked Brain Potentials (measured brain response that is the direct result of a specific cognitive event)
- Eye movement tracking: movements to first saccades
|
60 |
Female |
21 Years to 74 Years (Adult, Senior) |
NCT02770768 |
IRB16-0087 |
|
October 2016 |
June 2018 |
June 2018 |
May 12, 2016 |
April 4, 2017 |
|
- University of Chicago
Chicago, Illinois, United States
|
| 9 |
NCT02714049 |
Recruiting |
Flibanserin (Addyi®) vs. Flibanserin and Sex Therapy |
- Hypoactive Sexual Desire Disorder
|
- Behavioral: sex therapy
- Drug: flibanserin
|
Interventional |
Phase 4 |
- San Diego Sexual Medicine
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Desire domain of the Female Sexual Function Index (FSFI)
- Female Sexual Distress Scale (FSDS-DAO)
- Total score of the Female Sexual Function Index (FSFI)
|
60 |
Female |
18 Years and older (Adult, Senior) |
NCT02714049 |
SDSM-2015-03 |
|
January 2017 |
December 2018 |
March 2019 |
March 21, 2016 |
April 24, 2018 |
|
- San Diego Sexual Medicine
San Diego, California, United States
|
| 10 |
NCT03078829 |
Recruiting |
The Relation of GnRH Treatment to QTc Interval in Transgender Females |
|
- Drug: Treatment with a GnRh agonists
|
Observational |
|
- University of California, San Francisco
|
Other |
- Observational Model: Other
- Time Perspective: Prospective
|
- change in QTc Interval
- QTc interval > 450 milliseconds
|
23 |
Male |
10 Years and older (Child, Adult, Senior) |
NCT03078829 |
16-19936 |
|
March 2017 |
June 2019 |
January 2020 |
March 13, 2017 |
March 13, 2017 |
|
- University of California, San Francisco
San Francisco, California, United States
|
| 11 |
NCT02715232 |
Recruiting |
Effects of Sex Steroids on the Serotonin System |
|
- Drug: Testosterone
- Drug: Lynestrenol
- Drug: Cyproterone Acetate
- (and 2 more...)
|
Interventional |
Phase 4 |
- Medical University of Vienna
|
Other |
- Allocation: Non-Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Basic Science
|
- blood-to-brain clearance/trapping (K*) of [11C]AMT
- distribution volume (DV) of [11C]harmine
- white and gray matter microstructure
- (and 4 more...)
|
92 |
All |
18 Years to 50 Years (Adult) |
NCT02715232 |
1.1-20150511 |
|
February 6, 2017 |
December 2020 |
December 2020 |
March 22, 2016 |
April 13, 2017 |
|
- Department of Psychiatry and Psychotherapy, Medical University of Vienna
Vienna, Austria
|
| 12 |
NCT02958176 |
Recruiting |
Heart Rate Variability Biofeedback for Female Sexual Arousal Disorder |
- Female Sexual Arousal Disorder
|
- Behavioral: HRV Biofeedback
- Behavioral: Autogenic Training
|
Interventional |
Not Applicable |
- University of Texas at Austin
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Single (Participant)
- Primary Purpose: Treatment
|
- Physiological sexual arousal assessed by vaginal photoplethysmography
- Subjective sexual arousal assessed by Film Scale (Heiman & Rowland, 1983)
- Sexual function assessed by Female Sexual Function Index (Rosen et al., 2000)
- (and 3 more...)
|
65 |
Female |
18 Years to 40 Years (Adult) |
NCT02958176 |
2016-08-0074 |
|
October 2016 |
January 2018 |
January 2018 |
November 8, 2016 |
November 8, 2016 |
|
- The University of Texas at Austin
Austin, Texas, United States
|
| 13 |
NCT03287232 |
Recruiting |
Prasterone (DHEA) for the Treatment of Hypoactive Sexual Desire Disorder (HSDD) |
- Hypoactive Sexual Desire Disorder
|
- Drug: Placebo Vaginal Insert
- Drug: Prasterone 6.5 mg (0.50%) Vaginal Insert
|
Interventional |
Phase 3 |
|
Industry |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Primary Purpose: Treatment
|
- Sexual desire
- Distress from low sexual desire
- Satisfying sexual events (SSEs)
|
600 |
Female |
40 Years to 80 Years (Adult, Senior) |
NCT03287232 |
ERC-242 |
|
October 16, 2017 |
December 2018 |
March 2019 |
September 19, 2017 |
February 6, 2018 |
|
- Endoceutics site # 106
Huntsville, Alabama, United States - Endoceutics site # 104
Mobile, Alabama, United States - Endoceutics site # 117
Tucson, Arizona, United States - (and 58 more...)
|
| 14 |
NCT02968342 |
Recruiting |
Role of Progesterone in Hypoactive Sexual Desire Disorder in Menopausal Women |
- Menopause
- Sexual Desire Disorder
- Hypoactive Sexual Desire Disorder
|
- Device: Vaginal progesterone 8%
|
Interventional |
Phase 4 |
- Bezmialem Vakif University
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Single (Participant)
- Primary Purpose: Treatment
|
- FSFI (Female Sexual Function Index) questionnaire "arousal" domain
- FSFI (Female Sexual Function Index) questionnaire "lubrication" domain
- FSFI (Female Sexual Function Index) questionnaire all domains
- FSDS-R (Female Sexual Distress Scale- Revised) score
|
30 |
Female |
40 Years to 80 Years (Adult, Senior) |
NCT02968342 |
18.11.2015-21/35 |
|
July 2016 |
July 2018 |
July 2018 |
November 18, 2016 |
October 20, 2017 |
|
- Bezmialem Vakif University
Istanbul, Turkey
|
| 15 |
NCT03293771 |
Not yet recruiting |
Transgender Post-reassignment Urogynecologic Measures and Perceptions |
- Gender Identity Disorder of Adult
- Voiding Disorders
- Sexual Dysfunction
|
- Other: Focus group interviews
- Diagnostic Test: Questionnaire packet
|
Observational |
|
- Weill Medical College of Cornell University
|
Other |
- Observational Model: Other
- Time Perspective: Other
|
- Stage 1: Focus groups
- Stage 2: Questionnaire testing
- Frequency and severity of symptoms
- (and 3 more...)
|
200 |
Male |
18 Years and older (Adult, Senior) |
NCT03293771 |
1708018495 |
|
October 30, 2017 |
December 31, 2018 |
December 31, 2018 |
September 26, 2017 |
September 26, 2017 |
|
- Weill Cornell Medicine
New York, New York, United States
|
| 16 |
NCT03500406 |
Recruiting
New |
Penile Lengthening Pre-Penile Prosthesis Implantation |
|
- Device: RestoreX
- Other: Control
|
Interventional |
Not Applicable |
|
Other |
- Allocation: Randomized
- Intervention Model: Factorial Assignment
- Masking: Double (Investigator, Outcomes Assessor)
- Primary Purpose: Treatment
|
- Length Assessment of Penile Prosthesis Implanted
- Participant Compliance
- Participant Satisfaction with Traction
- (and 4 more...)
|
40 |
Male |
18 Years and older (Adult, Senior) |
NCT03500406 |
17-011052 |
|
March 23, 2018 |
March 23, 2021 |
March 23, 2021 |
April 17, 2018 |
April 17, 2018 |
|
- Mayo Clinic in Rochester
Rochester, Minnesota, United States - Washington University School of Medicine
Saint Louis, Missouri, United States
|
| 17 |
NCT03466619 |
Recruiting |
Penile Prosthesis in Patients With Erectile Dysfunction |
|
- Device: inflatable penile prosthesis (IPP)
|
Interventional |
Not Applicable |
|
Other |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Number of patients with improved erectile dysfunction
|
100 |
Male |
18 Years to 80 Years (Adult, Senior) |
NCT03466619 |
Khaled Hafez |
|
November 1, 2014 |
December 1, 2027 |
December 1, 2027 |
March 15, 2018 |
March 15, 2018 |
|
- Tanta university - faculty of medicine
Cairo, Elgharbia, Egypt
|
| 18 |
NCT03406169 |
Recruiting |
Erectile Recovery After Robotic-Assisted Laparoscopic Prostatectomy |
- Erectile Dysfunction
- Prostate Cancer
|
- Drug: Sildenafil 25 MG Oral Tablet
- Drug: Pentoxifylline
- Other: Placebo
|
Interventional |
Phase 3 |
- Brooke Army Medical Center
- Walter Reed National Military Medical Center
|
U.S. Fed |
- Allocation: Randomized
- Intervention Model: Single Group Assignment
- Masking: Triple (Participant, Care Provider, Investigator)
- Primary Purpose: Treatment
|
- Erectile function
- Penile length
|
180 |
Male |
30 Years to 89 Years (Adult, Senior) |
NCT03406169 |
C.2017.001 |
|
February 13, 2017 |
December 2021 |
March 2022 |
January 23, 2018 |
January 23, 2018 |
|
- Brooke Army Medical Center
San Antonio, Texas, United States
|
| 19 |
NCT03308409 |
Recruiting |
Comparative Effectiveness and Safety of Three Protocols Usin Li-ESWT for Erectile Dysfunction |
|
- Other: Low-intensity extracorporeal shock wave therapy (Li-ESWT)
|
Interventional |
Not Applicable |
|
Industry |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Single (Care Provider)
- Primary Purpose: Treatment
|
- IIEF-EF score 6 months after completing the treatment
- Erection Hardness Score
- Clinical improvement
- Number of satisfactory relations
|
279 |
Male |
18 Years and older (Adult, Senior) |
NCT03308409 |
LiWEST 3 protocols |
|
August 1, 2017 |
January 2019 |
August 2019 |
October 12, 2017 |
October 12, 2017 |
|
- Boston Medical Group
São Paulo, Brazil - Boston Medical Group Colombia
Bogotá, Cundinamarca, Colombia - Boston Medical Group
Mexico City, Mexico
|
| 20 |
NCT03222388 |
Recruiting |
Electronic IIEF Validation |
|
- Other: Questionnaire - IIEF 5/15
|
Observational |
|
- Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
- Société Internationale d'Urologie
|
Other |
- Observational Model: Case-Only
- Time Perspective: Prospective
|
- Reliability
- Preference for paper or electronic
|
172 |
Male |
40 Years and older (Adult, Senior) |
NCT03222388 |
17.281 |
|
July 25, 2017 |
October 1, 2017 |
October 14, 2017 |
July 19, 2017 |
August 11, 2017 |
|
- AMC University Hospital
Amsterdam, Noord-Holland, Netherlands
|
| 21 |
NCT03142542 |
Not yet recruiting |
The Efficacy and Safety of Udenafil in Patients With Erectile Dysfunction After Bilateral Nerve-sparing Radical Prostatectomy |
- Prostate Cancer With Radical Prostatectomy
|
- Drug: ZYDENA TAB.75mg(Udenafil 75mg)
- Drug: Placebo Oral Tablet
|
Interventional |
Phase 4 |
- Samsung Medical Center
- Dong-A ST Co., Ltd.
|
Other / Industry |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Triple (Participant, Care Provider, Investigator)
- Primary Purpose: Treatment
|
- The proportion of patients who has IIEF-EF score ≥22
- Safety evaulation: Occurrence of any adverse events
- Safety evaluation: Systolic and diastolic blood pressure
- (and 3 more...)
|
99 |
Male |
20 Years to 70 Years (Adult, Senior) |
NCT03142542 |
2017-02-112 |
DA8159_EDP_IIT |
May 2017 |
May 2019 |
December 2019 |
May 5, 2017 |
May 5, 2017 |
|
|
| 22 |
NCT03102762 |
Recruiting |
Botulinum Toxin for Erectile Dysfunction |
- Sexual Dysfunction
- Erectile Dysfunction
|
- Drug: Botulinum Toxin Type A
- Drug: Normal saline
|
Interventional |
Phase 2
Phase 3 |
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Double (Participant, Care Provider)
- Primary Purpose: Treatment
|
- Cavernosal Artery Mean PSV Before Treatment
- Cavernosal Artery Mean PSV After Treatment
- SHIM score before treatment
- (and 5 more...)
|
160 |
Male |
40 Years to 70 Years (Adult, Senior) |
NCT03102762 |
1232017 |
|
January 3, 2017 |
January 3, 2018 |
March 3, 2018 |
April 6, 2017 |
April 6, 2017 |
|
- Department of Andrology, Cairo University
Cairo, Egypt
|
| 23 |
NCT03102398 |
Recruiting |
A Study to Assess the Safety and Tolerability Profile of TR399 in Healthy Volunteers and Erectile Dysfunction Patients |
|
- Drug: TR-399 (5% Vardenafil HCl·3H2O, topical gel)
|
Interventional |
Phase 1
Phase 2 |
- Tritech Biopharmaceuticals Co., Ltd.
- A2 Healthcare Taiwan Corporation
|
Industry |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Safety evaluation of TR399 assessed by Incidence of AEs and SAEs
- Safety and efficacy evaluation of TR399 assessed by change from baseline to the last evaluation visit during the treatment period in score of IIEF-15 Erectile Function domain
- Safety evaluation of TR399 assessed by Maximum Plasma Concentration (Cmax)
- (and 10 more...)
|
26 |
Male |
20 Years to 70 Years (Adult, Senior) |
NCT03102398 |
TR399 |
|
March 31, 2017 |
January 31, 2018 |
March 31, 2018 |
April 5, 2017 |
November 22, 2017 |
|
- Mackay Memorial Hospital
Taipei, Taiwan
|
| 24 |
NCT03067987 |
Recruiting |
Safety and Efficacy of Low Intensity Shockwave for the Treatment of Erectile Dysfunction |
- Vasculogenic Erectile Dysfunction
|
- Device: Low Intensity Linear Shockwave Device for the Treatment of Erectile Dysfunction.
|
Interventional |
Not Applicable |
- University of Miami
- DIREX SYSTEMS CORPORATION
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- International Index of Erectile Function (IIEF-EF) Questionnaire
- Sexual Encounter profile (SEP)
- Global Assessment Question (GAQ)
- Erection Hardness Score (EHS)
|
80 |
Male |
30 Years to 80 Years (Adult, Senior) |
NCT03067987 |
20160964
20160335 |
|
February 22, 2017 |
June 22, 2018 |
September 22, 2018 |
March 1, 2017 |
January 24, 2018 |
|
- University of Miami
Miami, Florida, United States
|
| 25 |
NCT03039218 |
Recruiting |
Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED) |
|
- Device: Dornier Aries 2
- Device: Placebo / Sham
|
Interventional |
Not Applicable |
|
Industry |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Double (Participant, Investigator)
- Primary Purpose: Treatment
|
- International Inventory of Erectile Function ("IIEF")
|
100 |
Male |
22 Years to 70 Years (Adult, Senior) |
NCT03039218 |
G140216 S004 |
|
February 7, 2017 |
September 30, 2017 |
December 31, 2017 |
February 1, 2017 |
August 9, 2017 |
|
- San Diego Sexual Medicine
San Diego, California, United States - Adult Pediatric Urology & Urogynecology
Omaha, Nebraska, United States - Brooklyn Urology Research Group
Brooklyn, New York, United States - Manhattan Medical Research
New York, New York, United States
|
| 26 |
NCT03006536 |
Recruiting |
Low-Intensity Extracorporeal Shock Wave Treatment for Erectile Dysfunction: A Randomized, Controlled, Double Blind Trial |
|
|
Interventional |
Not Applicable |
- Zealand University Hospital
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Double (Participant, Investigator)
- Primary Purpose: Treatment
|
- International Index of Erectile Function (IIEF)
|
100 |
Male |
18 Years to 70 Years (Adult, Senior) |
NCT03006536 |
SJ-590 |
|
October 1, 2017 |
March 2019 |
March 2019 |
December 30, 2016 |
January 24, 2018 |
|
- Zealand University Hospital
Roskilde, Denmark
|
| 27 |
NCT02945449 |
Recruiting |
Use of Wharton Jelly in Erectile Dysfunction |
|
- Biological: Wharton Jelly Mesenchymal stem cells
|
Interventional |
Phase 1
Phase 2 |
- Sophia Al-Adwan
- University of Jordan
|
Other |
- Allocation: Non-Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
- Assessment of the efficacy of injecting Wharton Jelly derived Mesenchymal Stem Cells by Doppler Ultrasound test.
- Assessment of the efficacy of injecting Wharton Jelly derived Mesenchymal Stem Cells by SHIM/IIEF/EHS questionnaire
|
15 |
Male |
25 Years to 65 Years (Adult) |
NCT02945449 |
WJ.EDUJCTC |
|
January 4, 2017 |
September 2017 |
November 2017 |
October 26, 2016 |
May 8, 2017 |
|
- Cell Therapy Center
Amman, Jordan
|
| 28 |
NCT02943356 |
Recruiting |
Effect of Tadalafil on Erectile Dysfunction Treatment and QOL Improvement Effect (by SF-12) in Andropause Patients With Erectile Dysfunction |
- Erectile Dysfunction
- Andropause
|
|
Interventional |
Phase 4 |
- The Catholic University of Korea
- Hanmi Pharmaceutical Company Limited
|
Other / Industry |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Supportive Care
|
- Change on SF-12 Score from baseline to week 8
- Change on SF-12 Score from baseline to week 4
- Change on bioimpedance Analysis from baseline to week 8
- (and 2 more...)
|
40 |
Male |
35 Years and older (Adult, Senior) |
NCT02943356 |
TEDQOL |
|
July 2016 |
July 2017 |
July 2017 |
October 24, 2016 |
October 24, 2016 |
|
- Uijeongbu St.Mary's Hospital
Gyeonggi-do, Korea, Republic of
|
| 29 |
NCT02899572 |
Recruiting |
Impact of a Sexology Consultation on Disease Control of Type 2 Male Diabetics With Erectile Dysfunction |
- Erectile Dysfunction
- Type 2 Diabetes
|
- Procedure: Sexology consultation
|
Interventional |
Not Applicable |
- Centre Hospitalier Universitaire de la Réunion
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Measurement of HbA1c according to the randomisation group
|
64 |
Male |
18 Years to 65 Years (Adult) |
NCT02899572 |
2015/CHU/01 |
RADOTES |
June 2015 |
October 2016 |
January 2017 |
September 14, 2016 |
September 15, 2016 |
|
- Centre Hospitalier Gabriel Martin
Saint Paul, France
|
| 30 |
NCT02845765 |
Recruiting |
Fundus Oculi and Erectile Dysfunction |
|
- Device: Dynamic Vessel Analyzer (DVA)
- Drug: Phosphodiesterase type 5 Inhibitor (PDE5I)
|
Observational |
|
|
Other |
- Observational Model: Case-Control
- Time Perspective: Prospective
|
- Static and dynamic retinal vessels diameter
- International Index of Erectile Function (IIEF) Questionnaire
|
60 |
Male |
40 Years to 60 Years (Adult) |
NCT02845765 |
N.2015 FundusOculi_DE |
|
February 2016 |
January 2018 |
June 2018 |
July 27, 2016 |
October 10, 2017 |
|
- Ospedale San Raffaele
Milan, MI, Italy
|
| 31 |
NCT02798159 |
Recruiting |
Safety and Efficacy of TD0025 (Rocket1h) for Treatment of Erectile Dysfunction |
|
- Drug: TD0025
- Drug: Sildenafil Citrate 50mg
|
Interventional |
Phase 2
Phase 3 |
- Vietstar Biomedical Research
|
Industry |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Double (Participant, Investigator)
- Primary Purpose: Treatment
|
- PART A- PHASE II: Change From Baseline to 4 Weeks of the International Index of Erectile Function (IIEF), question # 3 and #4
- PART B- PHASE III: Change From Baseline to 4 Weeks of the International Index of Erectile Function (IIEF) Erectile Function (EF) Domain
- PART A- PHASE II: Change From Baseline to 4 Weeks of the International Index of Erectile Function (IIEF), Erectile Function (EF) Domain
- (and 18 more...)
|
168 |
All |
18 Years and older (Adult, Senior) |
NCT02798159 |
TD0025 |
TD0025 |
May 2016 |
February 2018 |
February 2018 |
June 14, 2016 |
November 6, 2017 |
|
- Men Sexual Health Centre; Vietnam- Germany Hospital
Hanoi, Vietnam
|
| 32 |
NCT02757807 |
Recruiting |
Stress Management Using an App to Improve Response With PDE5 Inhibitors in Men With Erectile Dysfunction. |
|
- Behavioral: Utilization of Serenita for Relaxation
|
Interventional |
Not Applicable |
|
Industry |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Global Assessment Profile measured by a survey
- Index of Erectile Function measured by a survey
|
100 |
Male |
18 Years to 55 Years (Adult) |
NCT02757807 |
008 |
|
July 2016 |
December 2016 |
December 2016 |
May 2, 2016 |
July 20, 2016 |
|
- RMA
New York, New York, United States
|
| 33 |
NCT02742896 |
Recruiting |
Evaluation for Restoration of Erectile Dysfunction After Cardioversion Treatment Trial |
|
- Other: Erectile dysfunction
|
Observational |
|
- Yong Seog Oh
- Seoul St. Mary's Hospital
|
Other |
- Observational Model: Cohort
- Time Perspective: Prospective
|
- The changes of erectile function
- The changes of cognitive function
|
358 |
All |
Child, Adult, Senior |
NCT02742896 |
ERECT |
|
December 2013 |
September 2017 |
November 2017 |
April 19, 2016 |
April 26, 2017 |
|
- Seoul St Mary's Hospital
Seoul, Seo Ch-gu, Korea, Republic of
|
| 34 |
NCT02683044 |
Recruiting |
Effectiveness And Safety Of Two Protocols For The Treatment Of Erectile Dysfunction With Low-Density Shock Waves |
|
- Procedure: Low-Intensity Extracorporeal Shock Wave Therapy (Li-ESWT)
|
Interventional |
Not Applicable |
- Instituto para la Evaluación de la Calidad y Atención en Salud
- Boston Medical Group
|
Other / Industry |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Erection Hardness Score (EHS)
- Penile blood flow
- International Index of Erectile Function, 5-item version (IIEF-5)
|
206 |
Male |
18 Years to 80 Years (Adult, Senior) |
NCT02683044 |
IECAS-BMG-01 |
|
February 2016 |
August 2017 |
December 2017 |
February 17, 2016 |
July 18, 2016 |
|
- Boston Medical Group
Bogota, Distrito Capital, Colombia
|
| 35 |
NCT02304679 |
Recruiting |
Low Energy Shockwave Therapy for Improving Erectile Dysfunction |
|
- Other: Pre-inclusion questionnaires
- Drug: 1 month of PDE5i treatment
- Other: PDE5i follow-up questionnaires
- (and 9 more...)
|
Interventional |
Not Applicable |
- Centre Hospitalier Universitaire de Nīmes
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Triple (Participant, Care Provider, Investigator)
- Primary Purpose: Treatment
|
- Change in IIEF-EF score
- % patients with improvement
- Change in IIEF-EF score from baseline
- (and 7 more...)
|
154 |
Male |
18 Years to 79 Years (Adult, Senior) |
NCT02304679 |
PHRC-N/2013/SD-01
2014-A00486-41 |
Shock-ED |
September 2015 |
November 2017 |
December 2018 |
December 2, 2014 |
June 20, 2016 |
|
- CHU de Bordeax - Hôpital Pellegrin
Bordeaux, France - APHP - Hôpital Raymond-Poincaré
Garches, France - Clinique Beau Soleil
Montpellier, France - (and 2 more...)
|
| 36 |
NCT01815593 |
Recruiting |
The Value of Enhanced External Counterpulsation on Erectile Dysfunction |
|
- Device: Enhanced external counterpulsation
|
Interventional |
Not Applicable |
- First Affiliated Hospital, Sun Yat-Sen University
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Erectile function evaluated by International Index of Erectile Function-5 questionnaire
- Endothelial function
|
120 |
Male |
18 Years to 80 Years (Adult, Senior) |
NCT01815593 |
EECPED |
EECPED |
April 2013 |
March 2018 |
April 2018 |
March 21, 2013 |
April 4, 2017 |
|
- First Affiliated Hospital, Sun Yat-sen University
Guangzhou, Guangdong, China
|
| 37 |
NCT01770340 |
Recruiting |
Nerve Grafting With an Allograft During Radical Prostatectomy - Extended Follow-up in a Prospective Randomized Trial |
- Erectile Dysfunction Following Radical Prostatectomy
|
- Biological: Radical prostatectomy with implantation of allograft
- Procedure: Radical prostatectomy without implantation of allograft
|
Interventional |
Phase 4 |
- Kantonsspital Winterthur KSW
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Single (Participant)
- Primary Purpose: Treatment
|
- Erectile function score (IIEF: international index of erectile function) after non nerve sparing radical prostatectomy
- Number of Participants with Adverse Events as a Measure of Safety and Tolerability
|
60 |
Male |
18 Years and older (Adult, Senior) |
NCT01770340 |
KEK-ZH-NR:2010-0004/0 |
|
January 2011 |
January 2017 |
January 2019 |
January 17, 2013 |
November 10, 2015 |
|
- Kantonsspital Winterthur
Winterthur, Kanton Zürich, Switzerland
|
| 38 |
NCT01249703 |
Recruiting |
The Early Diagnosis and Warning Role of Erectile Dysfunction |
- Erectile Dysfunction
- Endothelial Dysfunction
|
|
Observational |
|
- Sun Yat-sen University
- Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
|
Other |
- Observational Model: Case Control
|
|
150000 |
Male |
18 Years to 80 Years (Adult, Senior) |
NCT01249703 |
Chunhua Deng |
|
January 2008 |
October 2010 |
January 2020 |
November 30, 2010 |
November 30, 2010 |
|
- The First Affiliated Hospital of Sun Yat-Sen University
Guangzhou, Guang Dong, China
|
| 39 |
NCT02430987 |
Recruiting |
Prevalence of Metabolic Syndrome in Postmenopause Woman With Hypoactive Sexual Desire Disorder |
- Menopause
- Metabolic Syndrome
- Hypoactive Sexual Desire Disorder
|
|
Interventional |
Not Applicable |
- Faculdade de Ciências Médicas da Santa Casa de São Paulo
- Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.
|
Other |
- Allocation: Non-Randomized
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Prevention
|
- application of questionnaire
|
200 |
Female |
40 Years to 65 Years (Adult) |
NCT02430987 |
40594814.4.0000.5479 |
|
September 2014 |
June 2017 |
August 2017 |
April 30, 2015 |
May 15, 2017 |
|
- Faculdade de Ciências Médicas da Santa Casa de São Paulo
São Paulo, Brazil
|
| 40 |
NCT03192917 |
Not yet recruiting |
Low-energy Extracorporeal Shockwave Treatment for Patients After Radical Prostatectomy |
- Erectile Dysfunction
- Post-Op Complication
- Prostatic Diseases
|
- Procedure: Low intensity extracorporeal shock wave treatment (LI-ESWT)
- Procedure: Low intensity extracorporeal shock wave treatment (LI-ESWT) sham
|
Interventional |
Not Applicable |
- University of Southern Denmark
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Double (Participant, Investigator)
- Primary Purpose: Treatment
|
- Erection hardness score (EHS) Baseline
- Erection hardness score first follow up
- Erection hardness score second follow up
- (and 5 more...)
|
70 |
Male |
18 Years to 80 Years (Adult, Senior) |
NCT03192917 |
S-20170074 |
|
September 1, 2017 |
November 1, 2017 |
September 1, 2018 |
June 20, 2017 |
June 20, 2017 |
|
- Odense University Hospital (OUH)
Odense, Fyn, Denmark
|
| 41 |
NCT03427255 |
Recruiting |
CBT Group Treatment for Women With Dyspareunia |
|
- Behavioral: CBT group treatment-plus
- Other: Waiting-list control condition
|
Interventional |
Not Applicable |
- Örebro University, Sweden
- Leiden University Medical Center
- Maastricht University Medical Center
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Mean level of pain during penile/vaginal intercourse (PI)
- Penetration behavior questionnaire (PBQ)
- Genital pain rating questionnaire (GPQ)
- (and 8 more...)
|
160 |
Female |
18 Years to 45 Years (Adult) |
NCT03427255 |
CBT group program-plus |
|
September 29, 2017 |
December 31, 2019 |
December 31, 2019 |
February 9, 2018 |
February 9, 2018 |
|
- Leiden University Medical Center, Department of Gynecology
Leiden, Netherlands - Maastricht Universiy Medical Center (MUMC)
Maastricht, Netherlands - Center for Health and Medical Psychology (CHAMP) Örebro University
Örebro, Sweden
|
| 42 |
NCT03240081 |
Recruiting |
Treating Where it Hurts |
|
- Drug: 50mcg estradiol cream
- Drug: 100mcg estradiol cream
|
Interventional |
Phase 4 |
- Oregon Health and Science University
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Primary Purpose: Treatment
|
- Mean dyspareunia pain scores for intercourse at baseline and at weeks 4 and 12 after use of study drug
|
50 |
Female |
40 Years to 70 Years (Adult, Senior) |
NCT03240081 |
OHSU IRB 16770 |
|
June 20, 2017 |
June 30, 2018 |
January 31, 2019 |
August 4, 2017 |
August 4, 2017 |
|
- Oregon Health & Science Univerity
Portland, Oregon, United States
|
| 43 |
NCT03116022 |
Not yet recruiting |
Use of Estriol at Distal Third of Vagina Improving Coital Pain in Post-menopause Women |
- Dyspareunia
- Menopause
- Sexual Dysfunction
|
- Drug: Estriol
- Drug: Distal estriol
- Drug: Vaginal Gel
|
Interventional |
Phase 1 |
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Single (Investigator)
- Primary Purpose: Treatment
|
- Improvement in pain score after estriol use
- Number of participants with risk for sexual dysfunction after estriol use
- Number of participants with risk for anxiety after estriol use
- (and 9 more...)
|
132 |
Female |
40 Years to 65 Years (Adult) |
NCT03116022 |
62443916.5.0000.5440 |
|
June 1, 2017 |
December 31, 2018 |
January 31, 2019 |
April 14, 2017 |
April 14, 2017 |
|
|
| 44 |
NCT02739880 |
Recruiting |
Multi-point Intra-mucosal Injections of Cross-linked Hyaluronic Acid (DESIRIAL®) in the Vaginal Vestibule |
|
- Device: DESIRIAL® (Intra-mucosal Injections of Cross-linked Hyaluronic Acid)
|
Interventional |
Not Applicable |
- Centre Hospitalier Universitaire de Nīmes
- Laboratoires Vivacy
|
Other / Industry |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- The thickness of the vaginal mucosa on a histological section
- Vaginal pH
- Vaginal flora (on Pap smear)
- (and 6 more...)
|
20 |
Female |
18 Years to 69 Years (Adult, Senior) |
NCT02739880 |
LOCAL/2016/PM-001
2016-A00124-47 |
INREG 1 |
June 19, 2017 |
June 2018 |
June 2018 |
April 15, 2016 |
December 18, 2017 |
|
- CHRU de Nîmes - Hôpital Universitaire Carémeau
Nîmes Cedex 09, France - Centre Médical KARIS
Perpignan, France
|
| 45 |
NCT02484196 |
Not yet recruiting |
Dyspareunia in Women With Endometriosis: Impact of Surgery on Sexual Health |
|
- Behavioral: Questionnaires
|
Observational |
|
|
Other |
- Observational Model: Cohort
- Time Perspective: Prospective
|
|
100 |
All |
18 Years to 45 Years (Adult) |
NCT02484196 |
ENDODISP14 |
|
June 2016 |
June 2018 |
October 2018 |
June 29, 2015 |
March 9, 2016 |
|
|
| 46 |
NCT03194997 |
Not yet recruiting |
Pilates and Dance to Breast Cancer Patients Undergoing Treatment |
- Breast Cancer
- Quality of Life
- Lymphedema
- (and 13 more...)
|
- Other: Dance
- Other: Pilates
|
Interventional |
Not Applicable |
- Laboratório de Pesquisa em Lazer e Atividade Física
- Centro de Pesquisas Oncológicas
|
Other |
- Allocation: Randomized
- Intervention Model: Factorial Assignment
- Masking: Double (Participant, Investigator)
- Primary Purpose: Treatment
|
- Quality of life
- Depressive Symptoms
- Body image
- (and 16 more...)
|
201 |
Female |
18 Years and older (Adult, Senior) |
NCT03194997 |
2.073.549 |
|
January 1, 2018 |
July 30, 2018 |
July 30, 2020 |
June 22, 2017 |
August 16, 2017 |
|
|
| 47 |
NCT03178825 |
Recruiting |
Hybrid Fractional Laser for Symptoms of Genitourinary Syndrome of Menopause |
- Vaginal Atrophy
- Sexual Dysfunction
- Dyspareunia
- (and 2 more...)
|
- Device: Hybrid Fractional Laser
|
Interventional |
Not Applicable |
|
Industry |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Change from baseline in Vaginal Maturation Index (VMI)
- Change from baseline in Histology
- Change from baseline in Vaginal Health Index Score (VHIS)
- (and 3 more...)
|
60 |
Female |
40 Years to 70 Years (Adult, Senior) |
NCT03178825 |
DIVACIP002 |
|
May 19, 2017 |
October 21, 2018 |
October 30, 2018 |
June 7, 2017 |
September 26, 2017 |
|
- Women's Pelvic Health Institute
Los Gatos, California, United States - Coyle Institute
Pensacola, Florida, United States - Carolinas Healthcare System
Charlotte, North Carolina, United States - (and 2 more...)
|
| 48 |
NCT03290313 |
Not yet recruiting |
Clinical Trial Scheme of Shu Gan yi Yang Capsule |
- Depression With Erectile Dysfunction
|
- Drug: shu gan yi yang capsule
- Drug: shu gan yi yang capsule simulation agent
- Other: Supportive psychotherapy
|
Interventional |
Phase 4 |
- Beijing Hospital of Traditional Chinese Medicine
- Guizhou Yi Bai Pharmaceutical Co., Ltd.
- Peking University Sixth Hospital
- Beijing HuiLongGuan Hospital
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Double (Participant, Investigator)
- Primary Purpose: Treatment
|
- change of The international index of erectile function (IIEF-5) total score
- change of Montgomery Depression Rating Scale(MADRS)total score
- The change of total score of Hamilton Anxiety Scale (HAMA)
- (and 2 more...)
|
160 |
Male |
22 Years to 65 Years (Adult) |
NCT03290313 |
DHZD-SGYY |
|
September 2017 |
September 2018 |
December 2018 |
September 21, 2017 |
September 25, 2017 |
|
|
| 49 |
NCT03150225 |
Not yet recruiting |
Physical Exercise for Men With Andropause |
- Androgen Deficiency
- Depressive Symptoms
- Stress, Psychological
- (and 3 more...)
|
- Other: Concurrent training
|
Interventional |
Not Applicable |
- Laboratório de Pesquisa em Lazer e Atividade Física
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Triple (Participant, Investigator, Outcomes Assessor)
- Primary Purpose: Treatment
|
- Androgen deficiency in the aging male
- Cardiorespiratory fitness
- Body mass index
- (and 7 more...)
|
58 |
Male |
40 Years to 59 Years (Adult) |
NCT03150225 |
2.011.641 |
DAEM |
November 1, 2017 |
February 26, 2018 |
August 30, 2018 |
May 12, 2017 |
August 16, 2017 |
|
|
| 50 |
NCT03176069 |
Recruiting |
Evaluation and Comparison of Women Pelvic Floor With and Without Sexual Dysfunction (Vaginismus) |
- Vaginismus
- Sexual Dysfunctions
- Muscular Hypertonicity
- Muscle Tone Poor
|
- Other: Evaluation and Comparison of women pelvic floor with and without sexual dysfunction
- Other: The physiotherapeutic treatment
|
Interventional |
Not Applicable |
- Faculdade de Ciências Médicas da Santa Casa de São Paulo
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Single (Investigator)
- Primary Purpose: Other
|
- Quality sex life
- Female Sexual Function
- Verification of female anxiety
- (and 3 more...)
|
40 |
Female |
18 Years to 45 Years (Adult) |
NCT03176069 |
51995515.4.0000.5479 |
|
February 1, 2017 |
June 2017 |
February 2018 |
June 5, 2017 |
June 5, 2017 |
|
- Santa Casa of Sao Paulo Medical School
Sao Paulo, SP, Brazil
|
Create an RSS feed from your search for:
Download the search results for: