Clinical Trials Directory

Trials / Completed

CompletedNCT01262742

Carbetocin at Elective Cesarean Delivery

Carbetocin at Elective Cesarean Delivery: A Dose Finding Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Samuel Lunenfeld Research Institute, Mount Sinai Hospital · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

Post-partum hemorrhage (PPH) is a major cause of maternal death worldwide. Oxytocin is the most commonly uterotonic drug used to prevent and treat PPH in North America, however, there are some limitations to its use. Oxytocin has a very short duration of action, which requires a continuous infusion to achieve sustained uterotonic activity. The Society of Obstetricians and Gynecologists of Canada (SOGC) has recently recommended a single 100mcg dose of carbetocin at elective Cesarean delivery to promote uterine contraction and prevent post partum hemorrhage (PPH), in lieu of the more traditional oxytocin regimens. Carbetocin lasts 4 to 7 times longer than oxytocin, with a similar side effect profile and apparent greater efficacy rate. However, a dose response to determine the minimum effective dose of carbetocin has not yet been published. We hypothesize that a dose-response study will establish the minimum dose of carbetocin required to produce appropriate contractility in 95% of the women (ED95) undergoing elective cesarean delivery.

Detailed description

The Society of Obstetricians and Gynecologists of Canada (SOGC)recently recommended a 100mcg intravenous bolus dose of carbetocin following Cesarean delivery. However, a dose response study to determine the minimum effective dose of carbetocin has not yet been published. Studies thus far show that carbetocin may be just as effective as oxytocin in promoting uterine contraction, with a similar side effects profile. In addition, patients receiving carbetocin may experience less blood loss, and require less additional uterotonics when compared with oxytocin. The results of this study will define the minimum required dose of carbetocin for uterine contraction, thus minimizing unnecessary side effects, improving quality and safety of patient care. It may also contribute in establishing carbetocin as a substitute to oxytocin for elective cesarean section at our institution as well as others.

Conditions

Interventions

TypeNameDescription
DRUGCarbetocin80mcg carbetocin, IV, over 1 minute following delivery of the fetal head.
DRUGCarbetocin90mcg carbetocin, IV, over 1 minute following delivery of the fetal head.
DRUGCarbetocin100mcg carbetocin, IV, over 1 minute following delivery of the fetal head.
DRUGCarbetocin110mcg carbetocin, IV, over 1 minute following delivery of the fetal head.
DRUGCarbetocin120mcg carbetocin, IV, over 1 minute following delivery of the fetal head.

Timeline

Start date
2010-11-01
Primary completion
2011-03-01
Completion
2011-03-01
First posted
2010-12-17
Last updated
2025-04-25

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01262742. Inclusion in this directory is not an endorsement.