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NCT06765473Possibly a fitNot yet recruiting

Comparing Misoprostol before or after C-section to prevent heavy bleeding

Postpartum Hemorrhage

Treatments studied

Part of Women’s health & pregnancy clinical trials.

This study compares two ways of giving a medicine called misoprostol (which helps the womb contract) to prevent heavy bleeding after a C-section. One way is a vaginal tablet before surgery; the other is a tablet under the tongue after surgery. The goal is to find which way works better and is safer.

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

Phase
Phase 3
Enrollment
400 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are at least 37 weeks pregnant (full term).
  • You are having a planned C-section, not an emergency one.
  • Your baby's heartbeat is normal before the surgery.
  • You do not have placenta previa (placenta covering the cervix).
  • You have not had heavy bleeding after a previous birth.
  • You do not have a bleeding disorder or take blood thinners, and you are not on long-term steroids.

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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