Geneva, Aug. 6 -- International Clinical Trials Registry received information related to the study (NCT07728084) titled 'A Comparative Study Between Rectal and Intrauterine Misoprostol Administration in the Reduction of Blood Loss During and After Elective Cesarean Delivery in Low Risk Women' on July 21.

Study Type: Interventional

Study Design: Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Prevention. Masking: Single (Outcomes Assessor).

Primary Sponsor: Cairo University

Condition: Postpartum Hemorrhage, Cesarean Section

Intervention: Drug: Misoprostol Tabets

Recruitment Status: Not recruiting

Phase: N/A

Date of First Enrollment: January 13, 2025

Target Sample Size: 140

Countries of Rec...