To estimate the efficacy and safety of dried biological amnion graft after hysteroscopic lysis of intrauterine adhesions.
Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Subject) Primary Purpose: Prevention
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Enrollment
300
Uterine application of amnion membrane following hysteroscopic adhesiolysis. Other Name: Human amnion membrane
Device: Foley balloon Uterine application of Foley balloon
oral estradiol valerate tablets+dydrogesterone Tablets
Beijing Obstetrics and Gynecology Hospital,Capital Medical University
Beijing, Beijing Municipality, China
RECRUITINGsecond diagnostic hysteroscopy
Time frame: postoperation three to four months
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