Platelet Rich Plasma in the Prevention of Adhesion Reformation

NAEnrolling by invitationINTERVENTIONAL
Enrollment

46

Participants

Timeline

Start Date

October 10, 2023

Primary Completion Date

April 11, 2025

Study Completion Date

June 1, 2025

Conditions
Intrauterine AdhesionAsherman Syndrome
Interventions
BIOLOGICAL

PRP group

After the completion of hysteroscopic adhesiolysis, recruited participants will be randomized to one of the two treatment groups by computer-generated numbers: Immediately administer uterine perfusion with PRP after surgery, and administered PRP perfusion during hysteroscopy at 4 and 8 weeks after hysteroscopic adhesiolysis, A second-look hysteroscopy and ultrasound assessment of the endometrium will be carried out 4 weeks after the surgery, and again at 8 weeks after the surgery. Control group without PRP treatment.

Trial Locations (2)

100073

Fu Xing Hospital, Capital Medical University, Beijing

Fuxing hospital, Beijing

All Listed Sponsors
lead

Fu Xing Hospital, Capital Medical University

OTHER