Clin2
NCT07636421Possibly a fitRecruiting

Comparing two medications to prevent bleeding after planned C-section

Postpartum HemorrhageUterine AtonyCesarean SectionBlood Loss, Surgical

Treatments studied

Part of Women’s health & pregnancy clinical trials.

This trial tests two medicines given during a planned C-section to see which is better at preventing heavy bleeding. It may help make delivery safer for healthy women having a scheduled cesarean.

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

Phase
Phase 4
Enrollment
332 people
Ages
18 years to 45 years
Study type
Interventional

Who can take part

  • You are 18 to 45 years old and pregnant with one baby
  • You are at least 37 weeks pregnant
  • You are healthy (classified as ASA II) and having a planned (not emergency) C-section
  • Your hemoglobin (blood iron) level is 9 or higher
  • You can give written consent in Arabic or English

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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