Trial intelligence / Profile preview

Sublingual Misoprostol Before Hysteroscopic Resection of Symptomatic Uterine Niches

NCT07271056Completed

Sponsor
Benha University
Start
Feb 2025
Primary completion
Jul 2025
Modality
Small Molecules
Countries
1
01

Overview

Randomised, double-blind trial in cesarean scar defect (CSD), abnormal uterine bleeding (AUB) and cesarean section comparing Misoprostol group with Placebo group (2 arms). Primary endpoint: Reduction in number of days of postmenstrual spotting at 3 months. Started Feb 2025; status: completed.

02

Drugs

misoprostol
03

Conditions

cesarean scar defect (CSD)abnormal uterine bleeding (AUB)cesarean section

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