Clin2
NCT07688512Possibly a fitNot yet recruiting

Oxytocin dosing for high-risk C-section patients

Postpartum HemorrhageUterine AtonyUterine Atony With HemorrhageElective Cesarean Section

Part of Women’s health & pregnancy clinical trials.

This trial compares giving oxytocin as a single injection versus a slow drip during C-sections in people at high risk for heavy bleeding after delivery. The goal is to find which method works better to prevent postpartum hemorrhage.

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

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

Who can take part

  • You are having a planned cesarean section (not an emergency).
  • You will be awake with spinal anesthesia for the surgery.
  • You are considered high risk for heavy bleeding after delivery based on a standard checklist.
  • You can give consent in English or Spanish.

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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