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Trials / Completed

CompletedNCT02044549

Carbetocin Versus Syntometrine for Prevention of Postpartum Hemorrhage After Cesarean Section

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
300 (actual)
Sponsor
Cairo University · Academic / Other
Sex
Female
Age
18 Years – 39 Years
Healthy volunteers
Accepted

Summary

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

Detailed 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

Conditions

Interventions

TypeNameDescription
DRUGcarbetocinOxycontin analogue
DRUGSyntometrineUterotonins

Timeline

Start date
2014-06-01
Primary completion
2015-12-01
Completion
2015-12-01
First posted
2014-01-24
Last updated
2021-06-24

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT02044549. Inclusion in this directory is not an endorsement.

Carbetocin Versus Syntometrine for Prevention of Postpartum Hemorrhage After Cesarean Section (NCT02044549) · Clinical Trials Directory