drugset / Trial / NCT06009679

MISOPROSTOL FOR THE TREATMENT OF SUSPECTED POSTPARTUM RETAINED PRODUCTS OF CONCEPTION

NCT06009679

Unknown 150 enrolled Assuta Ashdod Hospital
RandomizedParallel-groupOpen-labelTreatment

Summary

The goal of this current study is to evaluate the efficacy of treatment of postpartum patients with suspected retained products of conception (RPOC) with Misoprostol in reducing the frequency of postpartum RPOC compared to a control group of patients that will be managed expectantly, in a prospective randomized trial.

Timeline

Start
2021-02-02
Primary completion
2024-12-31
Completion
2025-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Misoprostol Other / unclassified 600 ug Oral

Indications

No indication recorded.