Clin2
NCT07636421Likely a fitNot yet recruiting

Carbetocin alone versus carbetocin plus oxytocin for scheduled cesarean delivery

Postpartum HemorrhageUterine AtonyCesarean SectionBlood Loss, Surgical

Treatments studied

Part of Women’s health & pregnancy clinical trials.

This trial compares two medication approaches to prevent excessive bleeding during planned cesarean delivery under spinal anesthesia. Researchers want to see if one medication (carbetocin) works as well as carbetocin combined with a second medication (oxytocin).

Summary written for real people, not researchers, by Clin2.

Phase
Phase 4
Enrollment
332 people
Ages
18 years to 45 years
Study type
Interventional

Who can take part

  • You are an adult woman aged 18–45 years
  • You are scheduled for a planned (non-emergency) cesarean delivery
  • You will receive spinal anesthesia (numbing injection in your lower back) as your only anesthesia
  • You are carrying a single baby at 37 weeks of pregnancy or later
  • Your blood count (hemoglobin) is 9 g/dL or higher
  • You are generally healthy or have only mild, well-controlled medical conditions

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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