Clin2
NCT07188207Likely a fitNot yet recruiting

Rectal misoprostol to reduce blood loss during planned cesarean

Postpartum Hemorrhage

Treatments studied

Part of Women’s health & pregnancy clinical trials.

This trial tests if giving a medication called misoprostol as a rectal suppository can help reduce bleeding during a planned cesarean section. If you are having a planned cesarean and are generally healthy, this study might be an option for you.

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

Phase
N/A
Enrollment
282 people
Ages
18 years to 45 years
Study type
Interventional

Who can take part

  • You are between 18 and 45 years old.
  • You are pregnant with one baby and at least 37 weeks along.
  • You are scheduled for a planned cesarean section under spinal anesthesia.
  • You are in stable health before the surgery.
  • You do not have bleeding problems or take blood thinners.
  • You are not allergic to misoprostol or oxytocin.

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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