Clinical Trial

Balloon Tamponade Versus Gauze Packing for Postpartum Hemorrhage

Not Yet Recruiting
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Summary
Postpartum hemorrhage due to uterine atony is a major cause of maternal morbidity and mortality. This randomized controlled trial aims to compare the efficacy of uterine balloon tamponade and uterine gauze packing in controlling bleeding in women with postpartum hemorrhage. A total of 216 participants will be randomly assigned to one of the two treatment groups. All patients will receive standard medical management including uterotonic agents prior to intervention. The primary outcome is cessation of uterine bleeding within 24 hours after the procedure. This study aims to identify a safe and effective method for managing postpartum hemorrhage in a resource-limited setting.
Trial Details
NCT Number NCT07609589
Lead Sponsor Khyber Teaching Hospital
Conditions Postpartum Hemorrhage, Uterine Atony
Enrollment 216 participants
Start Date 2026-07-01
Primary Completion 2026-12-30 (estimated)
Study Completion 2027-01-10 (estimated)
Updated on ClinicalTrials.gov 2026-05-27