| 1 |
NCT03498443 |
Recruiting |
Effect of Pelvic Organ Prolapse Surgeries on Female Sexual Function in Egyptian Women |
- Female Sexual Dysfunction
|
|
Observational
|
|
|
Other |
- Observational Model: Case-Control
- Time Perspective: Prospective
|
- sexual function after prolapse surgeries
|
200 |
Female |
18 Years to 45 Years (Adult) |
NCT03498443 |
Asamir |
|
September 1, 2017 |
May 2018 |
May 1, 2018 |
April 13, 2018 |
April 13, 2018 |
|
- Benisuef Uneversity Hospital
Banī Suwayf, BeniSuef, Egypt
|
|
| 2 |
NCT02865187 |
Recruiting |
Evaluation of Vitamin D in Women With PCOS and Sexual Dysfunction |
- Female Sexual Dysfunction
- Polycystic Ovary Syndrome
|
- Dietary Supplement: Vitamin D
- Drug: Hormonal contraception
|
Interventional
|
Not Applicable |
- Wright State University
- Patty Brisben Foundation For Women's Sexual Health
|
Other |
- Allocation: Non-Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Sexual function
- Prevalence of sexual dysfunction in women with PCOS
|
60 |
Female |
18 Years to 40 Years (Adult) |
NCT02865187 |
Lindheim2016-01 |
Vit D in PCOS |
February 6, 2017 |
December 2018 |
December 2018 |
August 12, 2016 |
October 2, 2018 |
|
- Wright State Physicians
Dayton, Ohio, United States - Pennsylvania State University
Hershey, Pennsylvania, United States
|
|
| 3 |
NCT03172637 |
Not yet recruiting |
Female Sexual Dysfunction in Renal Failure |
- Evaluations of Sexual Dysfunction of Female in Chronic Renal Failure
|
|
Observational
|
|
- Esraa Ahmed Mohamed
- Assiut University
|
Other |
- Observational Model: Case-Control
- Time Perspective: Cross-Sectional
|
- effect of chronic renal failure in females on their sexuality function
|
100 |
Female |
18 Years to 45 Years (Adult) |
NCT03172637 |
FSDRF |
|
July 1, 2017 |
July 31, 2018 |
December 31, 2018 |
June 1, 2017 |
June 1, 2017 |
|
|
|
| 4 |
NCT03479229 |
Recruiting |
Viveve Geneveve Treatment of the Vaginal Introitus to Evaluate Safety and Efficacy |
- Female Sexual Dysfunction
|
- Device: Geneveve Treatment
- Device: Sham Treatment
|
Interventional
|
Not Applicable |
|
Industry |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Primary Purpose: Treatment
|
- Female Sexual Function Index (FSFI) Total Score
- Incidence of Treatment-Emergent Adverse Events
- Female Sexual Function Index (FSFI) Arousal Domain Score
- Female Sexual Function Index (FSFI) Orgasm Domain Score
|
250 |
Female |
18 Years and older (Adult, Older Adult) |
NCT03479229 |
VIVEVE II (VI-15-01) |
VIVEVE II |
April 20, 2018 |
December 2019 |
December 2019 |
March 27, 2018 |
May 17, 2018 |
|
- VIVEVE II Study Site
La Mesa, California, United States - VIVEVE II Study Site
Orange, California, United States - VIVEVE II Study Site
Denver, Colorado, United States - (and 18 more...)
|
|
| 5 |
NCT03500146 |
Recruiting |
Sexual Function Trial of Overactive Bladder: Medication Versus PTNS |
- Female Sexual Dysfunction
- Overactive Bladder
|
- Drug: Anticholinergic
- Procedure: PTNS
|
Observational
|
|
- Medstar Health Research Institute
- Indiana University
- University of Oklahoma
- University of Texas
|
Other |
- Observational Model: Cohort
- Time Perspective: Prospective
|
|
312 |
Female |
18 Years and older (Adult, Older Adult) |
NCT03500146 |
2016-248 |
STOMP |
January 30, 2017 |
June 30, 2018 |
December 30, 2018 |
April 17, 2018 |
April 17, 2018 |
|
- MedStar Washington Hospital Center
Washington, District of Columbia, United States - Indiana University
Indianapolis, Indiana, United States - University of Louisville
Louisville, Kentucky, United States - (and 2 more...)
|
|
| 6 |
NCT03427918 |
Recruiting |
The Effectiveness of the Mindfulness-based Cognitive Therapy (MBCT) on Sexual Functioning in Epileptic Women |
- Epilepsy
- Sexual Dysfunction
|
- Behavioral: Mindfulness-Based Sex Therapy
|
Interventional
|
Not Applicable |
- Qazvin University Of Medical Sciences
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Double (Investigator, Outcomes Assessor)
- Primary Purpose: Treatment
|
- Sexual functioning
- Intimacy
- sexuality-related distress
- (and 5 more...)
|
500 |
Female |
65 Years and older (Older Adult) |
NCT03427918 |
IR.QUMS.REC.1396.169 |
|
December 1, 2017 |
April 1, 2018 |
July 1, 2018 |
February 9, 2018 |
February 9, 2018 |
|
- Booali Sina Hospital
Qazvin, Iran, Islamic Republic of
|
|
| 7 |
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, Older Adult) |
NCT02859285 |
IRB # 15-18 |
|
April 2016 |
April 2018 |
December 31, 2018 |
August 9, 2016 |
September 21, 2017 |
|
- Waukesa Memorial Hospital
Waukesha, Wisconsin, United States
|
|
| 8 |
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, Older Adult) |
NCT03232801 |
PRO15060240
K23AG052628 |
|
January 2019 |
December 2019 |
December 2019 |
July 28, 2017 |
November 20, 2018 |
|
|
|
| 9 |
NCT03153631 |
Not yet recruiting |
Female Sexual Dysfunction in Breast Cancer Patients |
|
|
Observational
|
|
|
Other |
- Observational Model: Other
- Time Perspective: Prospective
|
- assessment of female sexual dysfunction in breast cancer patients after mastectomy using questionaire
|
75 |
Female |
18 Years to 40 Years (Adult) |
NCT03153631 |
fsdbc |
|
July 2017 |
July 2018 |
December 2018 |
May 15, 2017 |
May 16, 2017 |
|
|
|
| 10 |
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 |
May 21, 2018 |
|
- Алтайский государственный медицинский университет
Barnaul, Russian Federation - Kazan State Medical University
Kazan, Russian Federation - Kuban State Medical University
Krasnodar, Russian Federation - (and 17 more...)
|
|
| 11 |
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
|
|
| 12 |
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, Older Adult) |
NCT02968342 |
18.11.2015-21/35 |
|
July 2016 |
July 2018 |
July 2018 |
November 18, 2016 |
October 20, 2017 |
|
- Bezmialem Vakif University
Istanbul, Turkey
|
|
| 13 |
NCT03293771 |
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, Older Adult) |
NCT03293771 |
1708018495 |
|
December 27, 2017 |
December 31, 2018 |
December 31, 2018 |
September 26, 2017 |
August 2, 2018 |
|
- Weill Cornell Medicine
New York, New York, United States
|
|
| 14 |
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
|
|
| 15 |
NCT03372577 |
Recruiting |
Mindfulness-based Sex Therapy on Patients With Takotsubo Cardiomyopathy |
- Takotsubo Cardiomyopathy
- Sexual Dysfunction
|
- Behavioral: Mindfulness-Based Sex Therapy
- Other: Treatment as usual
|
Interventional
|
Not Applicable |
- Qazvin University Of Medical Sciences
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Double (Investigator, Outcomes Assessor)
- Primary Purpose: Treatment
|
- Sexual functioning
- Sexual Distress
- Intimacy
- (and 8 more...)
|
450 |
Female |
18 Years and older (Adult, Older Adult) |
NCT03372577 |
IR.QUMS.REC.1396.188 |
|
December 1, 2017 |
December 1, 2018 |
July 1, 2019 |
December 13, 2017 |
December 13, 2017 |
|
- Booali Sina Hospital
Qazvin, Iran, Islamic Republic of
|
|
| 16 |
NCT03780751 |
Recruiting |
Waitlist Controlled Comparison of Cognitive-behavioral vs. Mindfulness-based Online-treatments for Women With Low Sexual Desire |
- Hypoactive Sexual Desire Disorder
|
- Behavioral: Cognitive-behavioral treatment
- Behavioral: Mindfulness-based treatment
|
Interventional
|
Not Applicable |
- Ruhr University of Bochum
- Friedrich-Alexander-Universität Erlangen-Nürnberg
- University of British Columbia
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Sexual Interest and Desire Inventory Female (SIDI-F)
- Female Sexual Distress Scale Revised (FSDS-R)
|
266 |
Female |
18 Years and older (Adult, Older Adult) |
NCT03780751 |
VE 1083/2-1 |
MiSELF |
December 18, 2018 |
July 2021 |
January 2022 |
December 19, 2018 |
December 31, 2018 |
|
- Ruhr University Bochum
Bochum, NRW, Germany
|
|
| 17 |
NCT03775239 |
Recruiting |
Mindfulness as Treatment of Sexological Problems |
- Sexual Dysfunction
- Sexual Dysfunctions, Psychological
- Sexual Dysfunctions, Physiological
|
- Behavioral: Mindfulness in Sex Therapy and Intimate Relationships (MSIR)
- Behavioral: Treatment-as-usual
|
Interventional
|
Not Applicable |
- Mental Health Services in the Capital Region, Denmark
- Den Owesenske Fond
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- The Sexual Function Questionnaire for Females & Males (CSFQ-14-F/M)
- Female Sexual Function Index (FSFI)
- Female Sexual Distress Scale (FSDS)
- (and 6 more...)
|
30 |
All |
20 Years to 65 Years (Adult, Older Adult) |
NCT03775239 |
H-18017600 |
|
July 25, 2018 |
September 1, 2019 |
September 1, 2020 |
December 13, 2018 |
December 13, 2018 |
|
- Sexological Clinic
Copenhagen, Denmark
|
|
| 18 |
NCT03647189 |
Recruiting |
Randomized, Controlled Trial With Hybrid Fractional Laser |
- Vaginal Atrophy, Sexual Dysfunction, Vaginal Dryness, Dyspareunia
|
- Device: Hybrid Fractional Laser
|
Interventional
|
Not Applicable |
|
Industry |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Change from baseline in Vaginal health index score (VHIS)
- Change from baseline in Female sexual function index questionnaire (FSFI)
- Change from baseline in day-to-day impact of vaginal aging questionnaire
- (and 2 more...)
|
25 |
Female |
40 Years to 70 Years (Adult, Older Adult) |
NCT03647189 |
DIVA-001 |
|
August 10, 2018 |
March 2019 |
March 2019 |
August 27, 2018 |
September 6, 2018 |
|
- Miamim Dermatology
Miami, Florida, United States
|
|
| 19 |
NCT03782480 |
Recruiting
New |
Examining Effects of Intrarosa in Women With Genitourinary Syndrome of Menopause/Vulvovaginal Atrophy |
- Menopause
- Genitourinary Syndrome of Menopause
- Vulvovaginal Atrophy
- (and 2 more...)
|
- Drug: Intrarosa
- Drug: Placebos
|
Interventional
|
Phase 3 |
- Center for Vulvovaginal Disorders
- EndoCeutics Inc.
|
Other / Industry |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Primary Purpose: Treatment
|
- Changes from baseline in morphological content of vulvar and vaginal cells
- Changes from baseline in protein content of vulvar and vaginal cells
- Changes from baseline in enzymatic content of vulvar and vaginal cells
- (and 2 more...)
|
40 |
Female |
40 Years to 80 Years (Adult, Older Adult) |
NCT03782480 |
AGEC-10 |
|
January 2, 2019 |
January 2, 2021 |
January 2, 2021 |
December 20, 2018 |
December 20, 2018 |
|
- The Centers for Vulvovaginal Disorders
Washington, District of Columbia, United States - The Centers for Vulvovaginal Disorders
New York, New York, United States
|
|
| 20 |
NCT03682601 |
Recruiting |
Topical Treatment for Sexual Pain, Vulvar Pain, in Postmenopausal Women Not Taking Estrogens or Similiar Hormones |
- Sexual Pain Disorders
- Postmenopausal Symptoms
- Vulvovaginal Atrophy
- (and 5 more...)
|
- Drug: Sinecatechins Topical
- Other: Placebo
|
Interventional
|
Phase 4 |
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Primary Purpose: Treatment
|
- Numerical Rating Scale for pain
- Female Sexual Function Index Questionnaire;
- Female Sexual Distress Questionnaire revised
- (and 4 more...)
|
60 |
Female |
20 Years to 70 Years (Adult, Older Adult) |
NCT03682601 |
GTO1 |
|
August 30, 2018 |
June 30, 2019 |
September 30, 2019 |
September 24, 2018 |
November 28, 2018 |
|
- Lila Nachtigall, M.D.
New York, New York, United States
|
|
| 21 |
NCT03116022 |
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, Older Adult) |
NCT03116022 |
62443916.5.0000.5440 |
|
June 1, 2017 |
December 31, 2018 |
January 31, 2019 |
April 14, 2017 |
May 4, 2018 |
|
- Hospital das Clínicas de Ribeirão Preto
Ribeirão Preto, SP, Brazil
|
|
| 22 |
NCT03757975 |
Recruiting |
Impact of Hysterectomy on Quality of Life and Urethral Length |
- Fibroid Uterus
- Urethral Diseases
- Sex Disorder
|
- Procedure: urethral length measure
|
Observational
|
|
- Medical University of Lublin
|
Other |
- Observational Model: Case-Only
- Time Perspective: Cross-Sectional
|
- Change from Baseline urethral length at 6 months after hysterectomy
- Change from Baseline in sexual functions at 6 months after hysterectomy
- Change from Baseline in appearance of urinary incontinence at 6 months after hysterectomy
- (and 2 more...)
|
500 |
Female |
18 Years to 70 Years (Adult, Older Adult) |
NCT03757975 |
012018 |
|
July 1, 2018 |
July 31, 2019 |
August 31, 2019 |
November 29, 2018 |
November 29, 2018 |
|
- 2nd Gynecology Department
Lublin, Poland
|
|
| 23 |
NCT03163160 |
Recruiting |
Electrolysis Technique vs Manual Therapy in Pelvic Pain |
- Dyspareunia
- Pelvic Pain
- Pelvic Floor Disorders
- (and 2 more...)
|
- Procedure: Pelvic floor manual therapy group
- Procedure: Pelvic floor electrolysis group
|
Interventional
|
Not Applicable |
- Quirón Madrid University Hospital
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Single (Outcomes Assessor)
- Primary Purpose: Treatment
|
- Pain intensity before and after the intervention
- Female sexual function index
|
58 |
Female |
18 Years to 65 Years (Adult, Older Adult) |
NCT03163160 |
BET116183 |
|
June 20, 2017 |
December 20, 2018 |
December 20, 2019 |
May 22, 2017 |
November 9, 2018 |
|
- Hospital Universitario Quirón Madrid
Madrid, Spain
|
|
| 24 |
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
|
|
| 25 |
NCT03547089 |
Recruiting |
A Prospective Trial to Assess Breast Cancer Survivors and Vaginal Atrophy Treatment Outcomes |
- Vaginal Atrophy
- Genitourinary System; Disorder, Female
- Vaginal Abnormality
- (and 2 more...)
|
|
Interventional
|
Not Applicable |
- W. Grant Stevens, MD
- Marina Plastic Surgery
|
Other |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Sexual dysfunction
- Sexual distress
- Vaginal symptoms
- Vaginal laxity
|
10 |
Female |
18 Years and older (Adult, Older Adult) |
NCT03547089 |
VI-ISRP-026 |
BRAVO |
August 1, 2018 |
March 1, 2019 |
March 1, 2019 |
June 6, 2018 |
November 21, 2018 |
|
- Marina Plastic Surgery Associates
Marina Del Rey, California, United States
|
|
| 26 |
NCT01649089 |
Recruiting |
Studying the Physical Function and Quality of Life Before and After Surgery in Patients With Stage I Cervical Cancer |
- Cervical Adenocarcinoma
- Cervical Adenosquamous Carcinoma
- Cervical Squamous Cell Carcinoma, Not Otherwise Specified
- (and 5 more...)
|
- Procedure: Conization
- Other: Quality-of-Life Assessment
- Other: Questionnaire Administration
- (and 2 more...)
|
Interventional
|
Not Applicable |
- Gynecologic Oncology Group
- National Cancer Institute (NCI)
|
Other / NIH |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Supportive Care
|
- Change in bladder and bowel function score based on supplemental bladder and bowel questions plus 4 items from the Functional Assessment of Cancer Therapy-Cervix (3 bladder and 1 bowel question)
- Change in sexual function and activity based on Female Sexual Function Index (19 items) score plus 2 Patient Reported Outcomes Measurement Information System screener items
- Lymphedema
- (and 8 more...)
|
600 |
Female |
18 Years and older (Adult, Older Adult) |
NCT01649089 |
GOG-0278
NCI-2012-01990
CDR0000737208
U10CA101165
U10CA180868
UG1CA189867 |
|
October 1, 2012 |
February 1, 2021 |
|
July 25, 2012 |
May 10, 2018 |
|
- University of Arizona Cancer Center at Saint Joseph's
Phoenix, Arizona, United States - Saint Joseph's Hospital and Medical Center
Phoenix, Arizona, United States - Sutter Auburn Faith Hospital
Auburn, California, United States - (and 177 more...)
|
|
| 27 |
NCT02623244 |
Recruiting |
The Association Between Ovarian Endometrioma and Lower Urinary Tract Symptoms |
|
- Procedure: Laparoscopic oophorocystectomy or oophorectomy
|
Observational
|
|
- Far Eastern Memorial Hospital
|
Other |
- Observational Model: Case-Control
- Time Perspective: Prospective
|
- The association of ovarian endometrioma and overactive bladder symptoms score
- The association between ovarian endometrioma and female sexual function index score
- The association between ovarian endometrioma and bowel incontinence assessment score
|
90 |
Female |
20 Years and older (Adult, Older Adult) |
NCT02623244 |
104120-F |
|
November 6, 2015 |
September 30, 2019 |
October 1, 2019 |
December 7, 2015 |
May 22, 2018 |
|
- Far-Eastern Memorial Hospital
Banqiao, New Taipei, Taiwan
|
|
| 28 |
NCT03714581 |
Recruiting |
Laser Therapy Following Radiotherapy for Gynecological Cancer |
- Pelvic Radiotherapy
- Gynecological Cancer
- Dyspareunia
- Vaginal Dryness
|
- Device: Microablative Fractional CO2 Laser Therapy
|
Interventional
|
Not Applicable |
- National and Kapodistrian University of Athens
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Primary Purpose: Treatment
|
- 10-centimeter Visual Analogue Scale assessing intensity of dyspareunia and dryness
- 3 days voiding diary
- Day-to Day Impact of vaginal aging questionnaire (DIVA)
- (and 7 more...)
|
40 |
Female |
Child, Adult, Older Adult |
NCT03714581 |
143/21-03-2018 |
|
November 15, 2018 |
June 2019 |
June 2020 |
October 22, 2018 |
December 5, 2018 |
|
- Urogynecological Unit of Alexandra Hospital
Athens, Greece
|
|
| 29 |
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, Older Adult) |
NCT03365518 |
H17-02247
D2017-1893 |
INTROSPPECT |
December 29, 2017 |
December 2018 |
June 2019 |
December 7, 2017 |
October 16, 2018 |
|
- Gordon & Leslie Diamond Health Centre -- Vancouver General Hospital
Vancouver, British Columbia, Canada
|
|
| 30 |
NCT03681678 |
Recruiting |
Laser Therapy for Treatment of Urogenital Symptoms in Women |
- Genitourinary System; Disorder, Female
- Burning Vagina
- Dyspareunia
- (and 7 more...)
|
- Device: fCO2 Laser Therapy Group
|
Observational
|
|
- William Beaumont Hospitals
|
Other |
- Observational Model: Cohort
- Time Perspective: Prospective
|
- Change in Patient Global Impression of Improvement (PGI-I) score at 16 weeks (4 weeks post-initial treatment).
- Change in Patient Global Impression of Improvement (PGI-I) score
- Change in vaginal pH and overall vaginal health on physical exam as measured by the Vaginal Health Inventory Score (VHIS).
- (and 9 more...)
|
100 |
Female |
18 Years to 90 Years (Adult, Older Adult) |
NCT03681678 |
2018-142 |
|
October 8, 2018 |
June 2020 |
March 2021 |
September 24, 2018 |
January 11, 2019 |
|
- Beaumont Hospital
Royal Oak, Michigan, United States
|
|
| 31 |
NCT03257670 |
Recruiting |
Fractional CO2 Laser Therapy Versus 4% Topical Lidocaine Gel for Dyspareunia in Breast Cancer Survivors |
|
- Drug: 4% Topical Lidocaine Gel
- Device: CO2RE fractional laser therapy
|
Interventional
|
Not Applicable |
- University of Cincinnati
- Syneron Candela
|
Other / Industry |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Female Sexual Function Index (FSFI) score before and after treatment with topical lidocaine ointment or transvaginal CO2 laser among breast cancer survivors with dyspareunia.
- Numeric Pain Rating Scale (NPRS) score before and after treatment with topical lidocaine ointment or transvaginal CO2 laser among breast cancer survivors with dyspareunia.
- Incontinence Severity Index (ISI) score before and after treatment with topical lidocaine ointment or transvaginal CO2 laser among breast cancer survivors with dyspareunia.
- (and 5 more...)
|
70 |
Female |
18 Years and older (Adult, Older Adult) |
NCT03257670 |
UC Laser |
BCLS |
March 20, 2018 |
October 1, 2018 |
November 1, 2018 |
August 22, 2017 |
March 27, 2018 |
|
- University of Cincinnati
Cincinnati, Ohio, United States
|
|
| 32 |
NCT02495311 |
Recruiting |
The Association Between Adenomyosis/Uterine Myoma and Lower Urinary Tract Symptoms |
- Adenomyosis
- Uterine Leiomyoma
|
- Procedure: myomectomy or adenomyomectomy
|
Observational
|
|
- Far Eastern Memorial Hospital
|
Other |
- Observational Model: Case-Control
- Time Perspective: Prospective
|
- The corrleation coefficient between the size of myoma and Overactive Bladder Symptoms Scores
- The corrleation coefficient between the size of myoma and the presence of constipation/diarrhea
- Comparison of Overactive Bladder Symptoms Scores between the adenomyosis group and the control group
- Comparisons of the constipation/diarrhea rates between the adenomyosis group and the control group
|
150 |
Female |
20 Years and older (Adult, Older Adult) |
NCT02495311 |
103129-F |
|
November 15, 2014 |
December 31, 2020 |
December 31, 2020 |
July 13, 2015 |
November 5, 2018 |
|
- Far-Eastern Memorial Hospital
Banqiao, New Taipei, Taiwan
|
|
| 33 |
NCT03372720 |
Recruiting |
Fractional CO2 Laser Therapy in Minimizing Genitourinary Syndrome of Menopause in Gynecological Cancer Survivors |
- Cervical Carcinoma
- Dyspareunia
- Endometrial Carcinoma
- (and 4 more...)
|
- Procedure: Laser Therapy
- Other: Questionnaire Administration
- Procedure: Sham Intervention
|
Interventional
|
Not Applicable |
- Ohio State University Comprehensive Cancer Center
- National Cancer Institute (NCI)
|
Other / NIH |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Single (Participant)
- Primary Purpose: Supportive Care
|
- Change in genitourinary syndrome of menopause (GSM) symptoms
- Feasibility as measured by number of patients able to complete 3 study visitis
- Improvement in objective findings of vaginal atrophy
- (and 6 more...)
|
40 |
Female |
Child, Adult, Older Adult |
NCT03372720 |
OSU-17261
NCI-2017-02051
P30CA016058 |
|
March 28, 2018 |
December 31, 2020 |
December 31, 2020 |
December 14, 2017 |
August 28, 2018 |
|
- Johns Hopkins University
Baltimore, Maryland, United States - Mayo Clinic
Rochester, Minnesota, United States - Sanford Roger Maris Cancer Center
Fargo, North Dakota, United States - Ohio State University Comprehensive Cancer Center
Columbus, Ohio, United States
|
|
| 34 |
NCT03738605 |
Recruiting |
Vaginal Laser Therapy in Breast Cancer Survivors |
- Genitourinary Syndrome of Menopause
- Vaginal Atrophy
- Breast Cancer
- Dyspareunia
|
- Device: Microablative Fractional CO2 Laser Therapy
|
Interventional
|
Not Applicable |
- National and Kapodistrian University of Athens
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Primary Purpose: Treatment
|
- 10-centimeter Visual Analogue Scale assessing intensity of dyspareunia and dryness
- 3 days voiding diary
- Day-to Day Impact of vaginal aging questionnaire (DIVA)
- (and 13 more...)
|
50 |
Female |
Child, Adult, Older Adult |
NCT03738605 |
767/29-09-2017 |
|
December 1, 2018 |
June 2019 |
January 2020 |
November 12, 2018 |
December 11, 2018 |
|
- Urogynecological Unit of Alexandra Hospital
Athens, Greece
|
|
| 35 |
NCT03199534 |
Recruiting |
A Trial of Pelvic Floor Chemodenervation in Patients Undergoing Physical Therapy for High Tone Pelvic Floor Dysfunction |
- Pelvic Pain
- Dyspareunia
- Pelvic Floor Dysfunction
|
- Drug: Botulinum toxin A 50u
- Drug: Botulinum toxin A 100u
- Drug: Botulinum toxin A 150u
|
Interventional
|
Phase 4 |
- EvergreenHealth
- The Cleveland Clinic
|
Other |
- Allocation: Non-Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Change in Visual Analog Pain Scale (Non-Menstrual Pelvic Pain) score
- Visual Analog Pain Scale (Dyspareunia)
- Patient Global Impression of Severity
- (and 3 more...)
|
40 |
Female |
18 Years and older (Adult, Older Adult) |
NCT03199534 |
HTPFD |
|
May 25, 2017 |
January 2019 |
February 2019 |
June 27, 2017 |
January 8, 2018 |
|
- EvergreenHealth Urology and Urogynecology Care
Kirkland, Washington, United States
|
|
Create an RSS feed from your search for:
Download the search results for: