NCT05888545

Clinical Study on a Novel Anti-adhesion Barrier Film

A Randomized Controlled Study on an Anti-adhesion Diaphragm in Preventing Intrauterine Adhesions

• Status: Unknown
• Phase: N/A
• Study type: Interventional
• Enrollment: 1,176 (estimated)
• Sponsor: The Fourth Affiliated Hospital of Zhejiang University School of Medicine · Academic / Other
• Sex: Female
• Age: 18 Years – 40 Years
• Healthy volunteers: Not accepted

Summary

The aim of this clinical study was to verify the effectiveness and safety of the anti-adhesion diaphragm in preventing intrauterine adhesions.

Detailed description

The main questions it aims to answer are * The efficacy of the anti-adhesion diaphragm in preventing intrauterine adhesions; * The duration of placement of the anti-adhesion septum in the uterus. Participants will be asked to place an anti-adhesion diaphragm in the uterus for 3-7 days after the abortion procedure. The control group will receive conventional treatment with no other interventions. The researchers will compare the two groups to see if it is effective in clinical practice.

Conditions

• Intrauterine Adhesion

Interventions

Type	Name	Description
DEVICE	anti-adhesion diaphragm	Participants will be asked to place an anti-adhesion diaphragm in the uterus for 3-7 days after the abortion procedure.

Timeline

• Start date: 2023-04-01
• Primary completion: 2024-12-01
• Completion: 2024-12-31
• First posted: 2023-06-05
• Last updated: 2024-02-23

Locations

8 sites across 1 country: China