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The Efficacy and Safety of the Dried Biological Amnion Graft in Patients With Intrauterine Adhesions

NCT02496052 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2015-07-17

No results posted yet for this study

Summary

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

Conditions

  • Intrauterine Adhesions

Interventions

PROCEDURE

dried biological amnion graft

Uterine application of amnion membrane following hysteroscopic adhesiolysis. Other Name: Human amnion membrane

DEVICE

Foley balloon

Device: Foley balloon Uterine application of Foley balloon

DRUG

estradiol valerate tablets+dydrogesterone Tablets

oral estradiol valerate tablets+dydrogesterone Tablets

Sponsors & Collaborators

  • Beijing Obstetrics and Gynecology Hospital

    lead OTHER

Principal Investigators

  • Duan Hua, Ph.D · Beijing Obstetrics and Gynecology Hospital

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-01-31
Primary Completion
2017-01-31
Completion
2017-06-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02496052 on ClinicalTrials.gov