Clinical Trials Directory

Trials / Completed

CompletedNCT01630187

Comparison of Two Doses of Carbetocin for Prevention of Uterine Atony, During Elective Cesarean Section

Comparison of Two Doses of Carbetocin for Prevention of Uterine Atony During Elective Cesarean Section: a Randomized Controlled Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
72 (actual)
Sponsor
Laval University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the effectiveness of two doses of carbetocin (50 mcg vs 100 mcg) in preventing uterine atony during elective cesarean section.

Detailed description

Postpartum hemorrhage is a major cause of mortality and morbidity in the world, and it is most often caused by uterine atony. To prevent this complication, uterotonic medication is used during elective cesarean section. Carbetocin, a long-acting synthetic analogue of oxytocin, has been used for this purpose for many years. This medication has numerous side effects: hypotension, tachycardia, nausea, vomiting, chest pain, etc. Using a smaller dose of carbetocin might lower the incidence of these side effects, without compromising prevention of uterine atony in a low-risk group of patient.

Conditions

Interventions

TypeNameDescription
DRUGCarbetocinAdministration of carbetocin 50 mcg , after clamping the umbilical cord
DRUGCarbetocinAdministration of carbetocin 100 mcg , after clamping the umbilical cord

Timeline

Start date
2012-04-01
Primary completion
2012-07-01
Completion
2012-07-01
First posted
2012-06-28
Last updated
2013-05-29

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01630187. Inclusion in this directory is not an endorsement.