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A randomized clinical trial of preoperative versus postoperative misoprostol in elective cesarean delivery.

Int J Gynaecol Obstet

January 2016

Department of Obstetrics and Gynecology, College of Medicine, Qassim University, Buraydah, Saudi Arabia; Department of Obstetrics and Gynecology, College of Medicine, University of Bahri Suda, Khartoum, Sudan.

Objective: To determine the optimum time for misoprostol administration to minimize blood loss during and after elective cesarean delivery.

Methods: A randomized clinical trial was conducted at Mansoura University Hospital, Egypt, between January 1, 2013, and December 31, 2014. Eligible participants had full-term pregnancies, were scheduled to have a cesarean, and had normal fetal heart tracing.

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