A prospective, randomized, controlled, multicenter study on the prevention of adhesion after transcervical resection of septum

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000032061

Enrollment

Unknown

Registered

2020-04-19

Start date

2020-05-01

Completion date

Unknown

Last updated

2022-05-09

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

Conditions

septate uterus

Interventions

Placebo group:none

intrauterine stent group:uterine-shaped stent

estrogen group:estrogen

Eligibility

Sex/Gender

Female

Age

20 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Patients with confirmed septate uterus. 2. Women of childbearing aged less than 35 years old and not yet given birth.. 3. With regular menstruation and ovulation;

Exclusion criteria

Exclusion criteria: 1. Patients with double cervix or oblique vaginal septum. 2. Patients diagnosed as intrauterine adhensions. 3. Previous surgery history for uterine septum. 4. Patients with polycystic ovary syndrome. 5. Patients with hydrosalpinges. 6. Patients have severe adenomyosis or endometriosis.

Design outcomes

Primary

Measure	Time frame
intrauterine adhesion rate in second hysteroscopy;	—

Countries

China

Contacts

Public ContactLan Zhu

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences

zhu_julie@vip.sina.com+86 18612671818

Outcome results

None listed

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