Carbetocin Versus Syntometrine in Obese Women Undergoing Elective Cesarean

Status Completed

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 1200 obese pregnant subjected randomly either to single 100 μg IV dose of carbetocin (600 women) or combination of 5 IU oxytocin and 0.5 mg ergometrine (600 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

Clinical Trial Details

NCT number	NCT03693599
Study type	Interventional
Source	Cairo University
Contact
Status	Completed
Phase	Phase 4
Start date	October 1, 2018
Completion date	September 30, 2019

View Details

See also
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