Clinical Trial

Comparing Decidual Inclusion vs. Exclusion in Uterine Suture Techniques During Cesarean Section to Improve Scar Thickness and Reduce Isthmocele Risk in Primiparous Women

Study acronym: DISSUC
Not Yet Recruiting
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Summary
This study compares two ways of closing the uterus during cesarean delivery. In one group, the decidual layer near the uterine cavity is included in the suture. In the other group, this layer is left out. The study will examine whether these two methods differ in how well the uterine scar heals 6 to 9 months after surgery. Women having an elective cesarean delivery will be randomly assigned to one of the two closure methods. Scar healing will be assessed by ultrasound after delivery. The goal is to determine whether one method is associated with better cesarean scar healing and fewer scar defects.
Protocol Amendment History 1 change
critical Primary endpoint(s) modified 2026-06-02
Trial Details
NCT Number NCT07608874
Lead Sponsor Kantonsspital Baden
Conditions Isthmocele, Cesarean Scar Diverticula
Enrollment 374 participants
Start Date 2026-05-25
Primary Completion 2029-05-01 (estimated)
Study Completion 2029-05-30 (estimated)
Updated on ClinicalTrials.gov 2026-06-01