Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07271056Completed
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.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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