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Clinical Trial Summary

To estimate the efficacy and safety of dried biological amnion graft after hysteroscopic lysis of intrauterine adhesions.


Clinical Trial Description

Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Subject) Primary Purpose: Prevention ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT02496052
Study type Interventional
Source Beijing Obstetrics and Gynecology Hospital
Contact Wang Xin, MD
Phone 13681401510
Email wx_0327@126.com
Status Recruiting
Phase N/A
Start date January 2013
Completion date June 2017

See also
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Not yet recruiting NCT02132104 - Efficiency of Amnion Graft to Prevent Intrauterine Adhesions After Hysteroscopic Surgery N/A
Completed NCT02744807 - Role of Chronic Endometritis in Postoperative Recurrence of Severe Intrauterine Adhesions N/A
Terminated NCT01632202 - Seprafilm Slurry in the Prevention of Uterine Scarring in Patients Undergoing Hysteroscopic Myomectomy Phase 4
Recruiting NCT03731689 - Treatment of Intrauterine Adhesions and Its Distribution of Genital Tract Flora N/A
Not yet recruiting NCT02404454 - Prevention of Intrauterine Adhesions After Hysteroscopic Metroplasty With Autocross-linked Hyaluronic Acid Gel N/A
Recruiting NCT02204358 - Treatment of Infertility by Collagen Scaffold Loaded With Autologous Bone Marrow Stem Cells Phase 4