Trials / Completed
CompletedNCT04089176
Carbetocin Versus Oxytocin for Prevention of Postcesarean Hemorrhage in Pregnancy With High Risk for PPH
Carbetocin Versus Oxytocin for Prevention of Postcesarean Hemorrhage in Pregnant Women With High Risk Postpartum Hemorrhage: a Randomized Controlled Trial
- Status
- Completed
- Phase
- EARLY_Phase 1
- Study type
- Interventional
- Enrollment
- 120 (actual)
- Sponsor
- Department of Medical Services Ministry of Public Health of Thailand · Other Government
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
Objective: study efficacy of carbtocin versus oxytocin for prevention postpartum hemorrhage in high risk pregnancy who undergo cesarean section
Detailed description
Randomized controlled clinical trial. Defined patient in two group. Primary outcome is evaluate additional drug use Secondary outcome is evaluated estimated blood loss, hemoglobin level
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Carbetocin | carbetocin 100 mcg + RLS solution 10 ml injected directly into the vein over 2 min |
| DRUG | oxytocin | oxytocin 20 IU diluted in 1000 ml of RLS solution administered intravenously at rate 120 ml/hr x 8 hr |
Timeline
- Start date
- 2019-02-01
- Primary completion
- 2019-04-30
- Completion
- 2019-05-31
- First posted
- 2019-09-13
- Last updated
- 2019-09-13
Locations
1 site across 1 country: Thailand
Source: ClinicalTrials.gov record NCT04089176. Inclusion in this directory is not an endorsement.