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A Randomized Controlled Study of Uterine Incision Diverticulum Repair vs. no Repair During Second/Third Cesarean Section

StatusNot Yet Recruiting
PhaseNot applicable
Started2025-05-20
View on ClinicalTrials.gov ↗
Record status
This record was last updated May 21, 2025 (before its estimated June 1, 2026 completion). Its status may not reflect the trial's current state.
The goal of this study is to assess the efficacy and safety of uterine incision diverticulum repair during repeat cesarean section.The main questions it aims to answer are: * Can this surgical method improve the symptom of menorrhagia? * Is this procedure safe? Researchers will compare experimental group(Cesarean section + diverticulum repair group) to control group(Conventional cesarean section group) to see if this surgical method works to treat or improve menorrhagia. Participants will: * randomly assigned 1:1 to the experimental group(repairing uterine diverticula during cesarean section) and the control group (Routine cesarean section without repairing the uterine incision diverticulum) * visit the hospital 42 days after surgery * followed up by telephone 6-12 months after surgery

Amendment record

Amended once since 2024-09-23. Every amendment is listed below.

Dates here are the day the sponsor filed the amendment, not the day ClinicalTrials.gov published it. Version history last read from ClinicalTrials.gov on 2026-08-30.

2025-05-17
Amendment Study Status, Contacts/Locations v1
2024-09-23
Original filing
Trial Details
NCT Number NCT06612957
Lead Sponsor Shanghai First Maternal and Infant Health Hospital affiliated to Tongji University Medical School
Conditions Cesarean Scar Diverticulum
Enrollment 60 participants
Start Date 2025-05-20
Primary Completion 2026-06-01 (estimated)
Study Completion 2027-06-01 (estimated)
Updated on ClinicalTrials.gov 2025-05-21