Clinical Trials Directory

Trials / Completed

CompletedNCT04756661

Uterotonics for Severe Preeclampsia

Carbetocin Versus Combined Oxytocin and Misoprostol for Prevention of Postpartum Hemorrhage in Women With Severe Preeclampsia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
124 (actual)
Sponsor
Assiut University · Academic / Other
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

The study compares the effect of Intravenous carbetocin versus combined use of intravenous oxytocin and rectal misoprostol for prevention of postpartum hemorrhage during delivery of women with severe preeclampsia

Conditions

Interventions

TypeNameDescription
DRUGCarbetocin100 mcg of Carbetocin intravenous injection
DRUGOxytocin10 IU oxytocin IV drip
DRUGMisoprostol400 mcg rectal

Timeline

Start date
2020-01-01
Primary completion
2020-12-31
Completion
2021-02-10
First posted
2021-02-16
Last updated
2021-02-16

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04756661. Inclusion in this directory is not an endorsement.