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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

TypeNameDescription
DRUGIntravenous Oxytocin, Intravenous Tranexamic Acid, and Intramuscular Ergot DerivativeGroup 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
DRUGIntravenous Carbetocin aloneGroup 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.