drugset / Trial / NCT03556852

CARBETOCIN VERSUS RECTAL MISOPROSTOL FOR MANAGEMENT OF THIRD STAGE OF LABOR IN WOMEN AT LOW RISK OF POSTPARTUM HEMORRHAGE

NCT03556852

Phase 4 Completed 150 enrolled Cairo University
RandomizedParallel-groupTriple-blindPrevention

Summary

150 pregnant women admitted for spontaneous, induced or augmented vaginal delivery and categorized as low risk for postpartum hemorrhage (PPH) were divided randomly into two groups. Carbetocin group (C) received 1 ampoule of Carbetocin (100 μg/ml) (Pabal®, Draxis/Multipharma, Egypt, under license from DRAXIS PHARMA-Canada) added to 10 cc saline and given IV after the delivery of the baby. Misoprostol group (M) received 2 rectal misoprostol tablets (800 μg) (Misotac; SIGMA Pharm, Cairo, Egypt) after the delivery of the baby. Blood samples were tested to measure hemoglobin levels upon admission to the labor room and 12 hours after delivery

Timeline

Start
2018-07-02
Primary completion
2019-05-24
Completion
2019-05-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Carbetocin Peptide 100 ug/ml Intravenous
Comparator Misoprostol Other / unclassified 800 ug Rectal

Indications

No indication recorded.