Clin2
NCT07188207Likely a fitNot yet recruiting

Rectal misoprostol to reduce bleeding during planned cesarean section

Postpartum Hemorrhage

Treatments studied

Part of Women’s health & pregnancy clinical trials.

This study tests whether giving a medication (misoprostol) rectally during a planned C-section can help reduce blood loss after delivery. It may help women have a safer recovery with less bleeding.

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 (not twins or more) and at least 37 weeks along
  • Your C-section is planned and will use spinal anesthesia (you are awake but numb from the chest down)
  • Your blood pressure and heart rate are stable before surgery
  • You agree to participate and sign a consent form
  • You do not have heavy bleeding before surgery, blood-clotting problems, severe medical conditions like uncontrolled high blood pressure or heart disease, or an allergy to the study drug or similar medicines

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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