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The efficacy of auto-cross-linked gel in prevention of postoperative adhesion reformation: a randomised controlled trial

The efficacy of auto-cross-linked gel in prevention of postoperative adhesion reformation for patients with mild to moderate intrauterine adhesion: a randomised controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031713
Enrollment
Unknown
Registered
2020-04-08
Start date
2020-05-06
Completion date
Unknown
Last updated
2020-05-11

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

Conditions

Intrauterine Adhesion

Interventions

Experimental group:ACP Gel introduced after surgery
Control Group:No gel

Sponsors

Fuxing Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Aged 20-40 years; 2. Weight range from 50-80 kg; 3. Adhesion severity range from mild to moderate based on AFS score or ESGE classification; 4. Fully understand and willing to take part in this randomized controlled trial.

Exclusion criteria

Exclusion criteria: 1. previous history of endometrial tuberculosis; 2. previous history of uterine artery embolization; 3. patients with significant medical illnesses.

Design outcomes

Primary

MeasureTime frame
recurrence rate of intrauterine adhesion;severity of reformed adhesion;—

Secondary

MeasureTime frame
post-operative menstrual score;—

Countries

China

Contacts

Public ContactLi Tinchiu

Department of Hysteroscopic Centre, Fuxing Hospital, the Eighth Clinical Medical College, Capital Medical University, Beijing

13520279748@139.com+86 18613807887

Outcome results

None listed

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