Intrauterine balloon stent prevent adhesions recurrence

A clinical studies of Intrauterine balloon stent in th prevention of adhesion reformation following hysteroscopic surgery for Asherman syndrome

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-ICR-14005352

Enrollment

Unknown

Registered

2014-08-20

Start date

2013-10-20

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

intrauterine adhesion

Interventions

Experimental:placement of triangular uterine balloon catheter after hysteroscopic adhesiolysis

Control:hysteroscopic adhesiolysis

Eligibility

Sex/Gender

Female

Age

25 Years to 40 Years

Inclusion criteria

Inclusion criteria: the main cause of adhesion was curettage.

Exclusion criteria

Exclusion criteria: women age more-than 40 years, presence of infection including genital tuberculosis and significant medical disease.

Design outcomes

Primary

Measure	Time frame
Adhesion recurrence;	—

Secondary

Measure	Time frame
Menstrual pattern;endometrium;Abdominal pain;infection;Pregnancy outcomes;	—

Countries

China

Contacts

Public ContactWang Aiming

one_army@sina.com+86 18600310258

Outcome results

None listed

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