Trials / Completed
CompletedNCT02044549
Carbetocin Versus Syntometrine for Prevention of Postpartum Hemorrhage After Cesarean Section
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 300 (actual)
- Sponsor
- Cairo University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 39 Years
- Healthy volunteers
- Accepted
Summary
to compare effectiveness and tolerability of carbetocin versus syntometrine in prevention of Postpartum hemorrhage after cesarean section
Detailed description
A double blind randomized study conducted on 450 pregnant subjected randomly either to single 100 μg IV dose of carbetocin (150 women) or combination of 5 IU oxytocin and 0.2 mg ergometrine (300 women) after fetal extraction and before placental removal. Prevention of postpartum haemorrhage (PPH) after cesarean section (CS) had been evaluated by measurement of drop of Hemoglobin and hematocrit, incidence of PPH and number of subjects needed additional oxytocic
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | carbetocin | Oxycontin analogue |
| DRUG | Syntometrine | Uterotonins |
Timeline
- Start date
- 2014-06-01
- Primary completion
- 2015-12-01
- Completion
- 2015-12-01
- First posted
- 2014-01-24
- Last updated
- 2021-06-24
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT02044549. Inclusion in this directory is not an endorsement.