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398 studies found for:    Open Studies | "Uterine Diseases"
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21 Recruiting Stopping Heavy Periods Project
Conditions: Abnormal Uterine Bleeding;   Abnormal Uterine Bleeding, Ovulatory Dysfunction;   Abnormal Uterine Bleeding, Endometrial Hemostatic Dysfunction
Interventions: Device: Levonorgestrel intrauterine system;   Drug: Combined oral contraceptives
22 Recruiting Transvaginal Ultrasound in Women With Abnormal Uterine Bleeding
Condition: Abnormal Uterine Bleeding
Intervention: Device: Transvaginal sonography
23 Recruiting Anticipatory Counseling on LNG-IUS Continuation, Utilization and Satisfaction: A Pilot Study
Conditions: Vaginal Bleeding;   Uterine Cramping
Interventions: Other: Anticipatory Counseling;   Other: Cancer Screening Guidelines
24 Recruiting Prophylactic Bilateral Salpingectomy and Laparoscopic Myomectomy
Condition: Abnormal Uterine Bleeding, Unspecified
Interventions: Procedure: Prophylactic bilateral salpingectomy;   Procedure: Laparoscopic myomectomy without PBS
25 Recruiting Prospective Analysis of Restorelle in the Treatment of Uterine Prolapse
Condition: Uterine Prolapse
Intervention: Device: Restorelle Smartmesh
26 Recruiting Laparoscopic Supracervical Hysterectomy and Sacropexy Versus Hysteropexy Study
Condition: Uterus Prolapse
Interventions: Procedure: Laparoscopic Supracervical Hysterectomy and Sacropexy;   Procedure: Laparoscopic Hysteropexy
27 Recruiting Laparoscopic Sacral Colpopexy Versus Modified Total Pelvic Floor Reconstructive Surgery for Apical Prolapse Stage III-IV
Conditions: Uterine Prolapse;   Vault Prolapse
Interventions: Procedure: LSC;   Procedure: modified PFRS;   Device: "Gynemesh"
28 Not yet recruiting Treatment of Unfavorable Bleeding Patterns in Contraceptive Implant Users
Conditions: Bleeding;   Implants;   Breakthrough Bleeding
Interventions: Drug: Tamoxifen;   Drug: Placebo;   Drug: Tamoxifen (open label)
29 Not yet recruiting The Optimal Time for Intravenous Antibiotic Prophylaxis in Elective Cesarean Section
Condition: Endometritis
Intervention: Drug: ceftriaxone
30 Recruiting Preoperative Vaginal Cleansing With Povidone Iodine and the Risk of Post Cesarean Endometritis
Condition: Infection; Cesarean Section
Intervention: Drug: 10% povidone iodine
31 Recruiting RCT(Randomized Clinical Trial ) of Antibiotic Therapy in Chronic Endometritis
Condition: Chronic Endometritis
Interventions: Drug: antibiotics;   Drug: placebo
32 Recruiting Chronic Endometritis and IVF
Conditions: Chronic Endometritis;   in Vitro Fertilization
Intervention: Procedure: Endometrial biopsy
33 Recruiting Mirena Extension Trial
Condition: Contraception
Intervention: Drug: Levonorgestrel IUS (Mirena, BAY86-5028)
34 Not yet recruiting Librata Endometrial Ablation Device Treatment to Reduce Menstrual Blood Loss in Sites Across the United Kingdom
Condition: Heavy Menstrual Bleeding
Intervention: Device: Librata Endometrial Ablation
35 Recruiting A CLinical Study to Evaluate the Safety And Effectiveness of the CeRene DevIce to Treat HeavY Menstrual Bleeding
Condition: Menorrhagia
Intervention: Device: Cerene(TM) Cryotherapy Device
36 Recruiting Oral Tranexamic Acid Versus Diosmin for Treatment of Menorrhagia in Women Using Copper IUD
Condition: Menorrhagia
Interventions: Drug: Tranexamic Acid;   Drug: Diosmin
37 Recruiting Ultrasound Appearance of the Endometrium Post Radio-Frequency Ablation
Condition: Menorrhagia
Intervention: Other: Ultrasound
38 Recruiting Copper IUD Treatment Observation Study
Condition: Menorrhagia
Interventions: Drug: Naproxen;   Drug: Placebo
39 Recruiting A Study to Evaluate the Effectiveness of Essure Post-NovaSure Radiofrequency Endometrial Ablation Procedure Following a Successful Essure Confirmation Test
Conditions: Contraception;   Menorrhagia
Interventions: Device: ESS305 (Essure, BAY1454032);   Procedure: NovaSure
40 Not yet recruiting Quality of Life Outcomes for Ulipristal Acetate and Tranexamic Acid in the Management of Heavy Menstrual Bleeding
Condition: Heavy Menstrual Bleeding
Interventions: Drug: UPA;   Drug: TEA;   Drug: Placebo (for UPA);   Drug: Placebo (for TEA)

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Study has passed its completion date and status has not been verified in more than two years.