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Clinical Trials/ISRCTN69690272
ISRCTN69690272
Completed
Not Applicable

A comparison of intrauterine balloon stent and intrauterine contraceptive device in the prevention of adhesion reformation following hysteroscopic surgery for Asherman syndrome: a randomized case-control study

Health Bureau of Zhejiang Province (China)0 sites200 target enrollmentFebruary 15, 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Asherman syndrome
Sponsor
Health Bureau of Zhejiang Province (China)
Enrollment
200
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 15, 2013
End Date
TBD
Last Updated
9 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Health Bureau of Zhejiang Province (China)

Eligibility Criteria

Inclusion Criteria

  • 1\. Woman with confirmed uterine adhesion with moderate or severe degree \[American Fertility Society (AFS score range 5\~12\)] by hysteroscopic examination and history review for the first time in Sir Run Run Shaw hospital is to be recruited.
  • 2\. All the participants should be \>\=18 years and younger than 40 years old, having potential conceiving requirement

Exclusion Criteria

  • 1\. Older than 40 years old
  • 2\. The AFS score less than 5
  • 3\. Who doesn't want to get pregnant
  • 4\. Who has received hysteroscopic adhesive resection before
  • 5\. Who can't follow up according to the study protocol

Outcomes

Primary Outcomes

Not specified

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