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Prospective, randomized, controlled trial comparing the efficacy and security of intrauterine balloon placement duration in preventing of adhesion reformation after sever degree hysteroscopic adhesiolysis

Prospective, randomized, controlled trial comparing the efficacy and security of intrauterine balloon placement duration in preventing of adhesion reformation after sever degree hysteroscopic adhesiolysis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-ICR-15007339
Enrollment
Unknown
Registered
2015-11-03
Start date
2015-11-20
Completion date
Unknown
Last updated
2020-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intrauterine adhesions

Interventions

3:placing intrauterine balloon twenty-eight days
1:placing intrauterine balloon seven days
2:placing intrauterine forteen days

Sponsors

Fuxing Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. The bearing-age women with sever degree intrauterine adhesion (IV and V degree); 2. Without reproductive system malformation and without endometrial lesions who were preoperative pathologic examination; 3. To agree and sign the informed consent; 4. Agree to have second-look hysteroscopy.

Exclusion criteria

Exclusion criteria: 1. Unable to accept hysteroscopy surgery with some diseases; 2. With acute or chronic genital tract inflammation; 3. Patients have the contraindications of the hormone therapy drug.

Design outcomes

Primary

MeasureTime frame
Incidence of adhesion reformation ;the intrauterine adhesion rate;—

Secondary

MeasureTime frame
menstruation;the pregancy;—

Countries

China

Contacts

Public ContactLiu Yuhuan

Fuxing Hospital, Capital Medical University

liuyh3844@sina.com+86 13801133844

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026