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NCT06333340Possibly a fitRecruiting

Comparing two medicines to prevent heavy bleeding after planned cesarean

Post Partum Hemorrhage

Treatments studied

Part of Women’s health & pregnancy clinical trials.

This study compares two medicines—carbetocin and oxytocin—given during a planned cesarean to help prevent heavy bleeding after delivery. It is for women who have certain risk factors for uterine atony (when the uterus does not tighten up after birth).

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

Phase
N/A
Enrollment
160 people
Ages
18 years to 50 years
Study type
Interventional

Who can take part

  • You are scheduled for a planned (elective) cesarean section.
  • You have at least one of the following risk factors: a larger than normal uterus (from too much amniotic fluid, a big baby, or multiple babies), a history of heavy bleeding after a previous birth, obesity with a BMI over 40, diabetes or high blood pressure on medication, or placenta previa.
  • You do not have any heart valve problems, irregular heartbeat, or heart failure.
  • You do not have placenta accreta (a condition where the placenta grows too deeply).
  • You do not have a bleeding disorder or severe anemia (hemoglobin below 100 g/L).
  • You are not allergic to oxytocin or carbetocin.

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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