Viewing Study NCT06612957



Ignite Creation Date: 2024-10-26 @ 3:41 PM
Last Modification Date: 2024-10-26 @ 3:41 PM
Study NCT ID: NCT06612957
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-09-23

Brief Title: A Randomized Controlled Study of Uterine Incision Diverticulum Repair vs no Repair During SecondThird Cesarean Section
Sponsor: None
Organization: None

Study Overview

Official Title: A Randomized Controlled Study of Uterine Incision Diverticular Repair During Repeated Cesarean Section
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this study is to assess the efficacy and safety of uterine incision diverticulum repair during repeat cesarean sectionThe main questions it aims to answer are

Can this surgical method improve the symptom of menorrhagia
Is this procedure safe Researchers will compare experimental groupCesarean section diverticulum repair group to control groupConventional cesarean section group to see if this surgical method works to treat or improve menorrhagia

Participants will

randomly assigned 11 to the experimental grouprepairing 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None