A randomized controlled clinical trial of the efficacy of estrogen therapy after hysteroscopic adhesiolysis of intrauterine adhesions

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-IPR-15007113

Enrollment

Unknown

Registered

2015-01-01

Start date

2015-01-01

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

interuterine adhesion

Interventions

Experimental group:Sex hormone

Control group:no sex hormone

Eligibility

Sex/Gender

Female

Age

20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Patients with intrauterine adhesions are caused by repeatedly intrauterine mechanical operations; 2. Patients are diagnosised with intrauterine adhesions by Hysteroscopy; 3. Patients have fertility requirements; 4. Patients all are voluntared to participate in the trial.

Exclusion criteria

Exclusion criteria: 1. age>40year; 2. no fertility requirements; 3. Intrauterine adhesions without mechanical intrauterine operations, as Tuberculous intrauterine adhesions, Uterine artery embolization; 4. Untreated male infertility; 5. Patients with untreated uterine diseases, which affect fertility; 6. Patients with dinseases which is ot suitable for applications of sex hormone; 7. no hormone used in the past 3 months.

Design outcomes

Primary

Measure	Time frame
reformation of intrauterine adhesions;Menstruation;Implantation rate;	—

Secondary

Measure	Time frame
Pregnancy outcome;Endometrial thickness;Incidence of adverse reactions;Conceive Method;Preoperative levels of sex hormones;Pregnancy history;Number of intrauterine operations;	—

Countries

China

Contacts

Public Contactaiming wang

1073962381@qq.com+86 18600310258

Outcome results

None listed

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