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
| Type | Name | Description |
|---|---|---|
| DRUG | Carbetocin | Administration of carbetocin 50 mcg , after clamping the umbilical cord |
| DRUG | Carbetocin | Administration 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.