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Clinical Trials/NCT02867202
NCT02867202
Completed
Not Applicable

A Randomized Clinical Trial to Assess the Efficacy of Intrauterine Balloon Compared to Intrauterine Contraceptive Device Plus Foley Catheter in the Therapy for Uterine Adhesion After Hysteroscopic Adhesiolysis

Wenzhou Medical University1 site in 1 country171 target enrollmentJune 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Asherman Syndrome
Sponsor
Wenzhou Medical University
Enrollment
171
Locations
1
Primary Endpoint
the AFS Score at Second-look Hysteroscopy
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This study was taken out to compare two mechanical devices (intrauterine balloon and Intrauterine Contraceptive Device Plus Foley Catheter) in the therapy for intrauterine adhesions after hysteroscopic adhesiolysis. Participates were assigned into two groups by randomly.

Detailed Description

Intrauterine balloon and Intrauterine Contraceptive Device Plus Foley Catheter are both effective in the therapy for intrauterine adhesion. The Intrauterine Contraceptive Device Plus Foley Catheter are usually inserted into the uterine after hysteroscopic adhesiolysis. Foley Catheter is removed after three days while intrauterine device is removed two or three month later. The heart-shaped intrauterine balloon is designed to fit into the cavity of the uterus, and usually removed on the 7th day after surgery.

Registry
clinicaltrials.gov
Start Date
June 2015
End Date
December 2017
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Feng Lin

attending doctor

Wenzhou Medical University

Eligibility Criteria

Inclusion Criteria

  • Moderate to severe intrauterine adhesion (AFS score ≥5)
  • Agreement to have a second-look hysteroscopy
  • no previous history of hysteroscopic adhesiolysis

Exclusion Criteria

  • Minimal adhesion (AFS score\<5)
  • Previous hysteroscopic adhesiolysis

Outcomes

Primary Outcomes

the AFS Score at Second-look Hysteroscopy

Time Frame: 2 or 3 months after the surgery

The AFS score is based on the American Fertility Society (AFS) Classification of Intra-uterine adhesions( 1988 version)The total range of AFS score is from 0 to 12, and the higher the score is, the worse the outcome is.

Study Sites (1)

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