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NCT06560099Possibly a fitNot yet recruiting

Comparing two oxytocin doses for bleeding control in high-risk cesarean births

Post Partum Hemorrhage

Treatments studied

Part of Women’s health & pregnancy clinical trials.

This study compares two doses of oxytocin (a medicine given during cesarean section to prevent heavy bleeding) to see which works better for women with high-risk pregnancies. If you are having a planned cesarean and have certain risk factors, this trial may help find the best dose for you.

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

Phase
N/A
Enrollment
39 people
Ages
20 years to 45 years
Study type
Interventional

Who can take part

  • You are scheduled for a planned (not emergency) cesarean section.
  • You have a condition that makes this a high-risk pregnancy – like high blood pressure, diabetes, a blood disorder, placenta problem, or carrying twins.
  • You may have had heavy bleeding after a past birth, or have a history of infertility treatment or endometriosis.
  • You are not allergic to oxytocin (a medicine that helps the womb contract).
  • You did not already have labor contractions before the cesarean (exhausted uterus) or a condition called Couvelaire uterus.
  • You are not on medicines that prevent blood clots (like blood thinners) unless your doctor approves.

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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