A prospective study on the factors affecting the efficacy of hysteroscopic adhesiolysis

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2100045479

Enrollment

Unknown

Registered

2021-04-17

Start date

2021-04-19

Completion date

Unknown

Last updated

2021-11-29

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

Conditions

intrauterine adhesion

Interventions

moderate adhesion group:Nil

severe adhesion group:Nil

Eligibility

Sex/Gender

Female

Age

20 Years to 38 Years

Inclusion criteria

Inclusion criteria: 1. Aged 20-38 years; 2. Height and body mass index 18.5-30 Kg/m2; 3. Moderate to severe intrauterine adhesions, preoperative AFS score >= 5 points; 4. Regular menstrual cycle, 21-35 days; 5. There are fertility requirements; 6. Volunteer to join the study, agree to the treatment plan and postoperative follow-up.

Exclusion criteria

Exclusion criteria: 1. Those with a history of genital tuberculosis; 2. Patients with severe medical and surgical diseases, tumors and patients with family history of tumors; 3. Patients with contraindications to hormone use.

Design outcomes

Primary

Measure	Time frame
Uterine adhesion severity score;	—

Secondary

Measure	Time frame
adhesion recurrence rate;pregnancy rate;endometrial receptivity;	—

Countries

China

Contacts

Public ContactLuo Yiyang

Fuxing Hospital, Capital Medical University

luoyiyang2011@sina.com13810245053

Outcome results

None listed

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