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Clinical Trial Summary

to compare effectiveness and tolerability of carbetocin versus syntometrine in prevention of Postpartum hemorrhage after cesarean section


Clinical Trial Description

A double blind randomized study conducted on 450 pregnant subjected randomly either to single 100 μg IV dose of carbetocin (150 women) or combination of 5 IU oxytocin and 0.2 mg ergometrine (300 women) after fetal extraction and before placental removal. Prevention of postpartum haemorrhage (PPH) after cesarean section (CS) had been evaluated by measurement of drop of Hemoglobin and hematocrit, incidence of PPH and number of subjects needed additional oxytocic ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02044549
Study type Interventional
Source Cairo University
Contact
Status Completed
Phase Phase 4
Start date June 2014
Completion date December 2015

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