Overview

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

Status:
Completed
Trial end date:
2012-07-01
Target enrollment:
0
Participant gender:
Female
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.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Laval University
Treatments:
Carbetocin
Oxytocin
Criteria
Inclusion Criteria:

- ≥ 18 years old

- ≥ 37-week pregnancy

- singleton pregnancy

- elective cesarean section with a low transverse incision

- ASA I or II

Exclusion Criteria:

- Personal history of uterine atony or postpartum hemorrhage

- Abnormal placental implantation (known or suspected)

- > 3 cesarean sections in the past

- Personal history of a classic uterine incision

- Estimated fetal weight > 4500g

- Hemoglobin < 100 g/L

- Regular use of tocolytic drugs

- Cesarean section under general anesthesia

- Known allergy to carbetocin

- Refusal

- Inability to obtain informed consent