Trials / Not Yet Recruiting
Not Yet RecruitingNCT07318467
Prophylactic Regimen of Intravenous Oxytocin, Intravenous Tranexamic Acid, and Intramuscular Ergot Derivative for Primary Prevention of Postpartum Hemorrhage in Intrapartum Cesarean Section Versus Intravenous Carbetocin Alone
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 80 (estimated)
- Sponsor
- Cairo University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
While Carbetocin is effective in reducing PPH, the combination of oxytocin, Tranexamic acid, and Ergot derivatives may offer additional benefits in high-risk populations. We hypothesize that the combination regimen will reduce PPH incidence and severity compared to Carbetocin alone and may be more cost effective
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Intravenous Oxytocin, Intravenous Tranexamic Acid, and Intramuscular Ergot Derivative | Group A will receive a combination regimen of intravenous Oxytocin (5-10IU), Tranexamic acid (intravenous bolus 1 gram), and intramuscular ergot derivative (methylergometrine maleate 0.2 mg/ ml). The participants will receive intravenous Oxytocin immediately after delivery of the fetus, intravenous Tranexamic acid during the procedure and intramuscular Ergot derivative after delivery of the placenta |
| DRUG | Intravenous Carbetocin alone | Group B will receive intravenous Carbetocin (100 mcg) only. The participants will receive intravenous Carbetocin only immediately after delivery of the fetus. |
Timeline
- Start date
- 2026-01-01
- Primary completion
- 2026-06-30
- Completion
- 2026-06-30
- First posted
- 2026-01-06
- Last updated
- 2026-01-06
Source: ClinicalTrials.gov record NCT07318467. Inclusion in this directory is not an endorsement.