Clin2
NCT07688512Possibly a fitNot yet recruiting

Oxytocin dosing for women at risk of bleeding after C-section

Postpartum HemorrhageUterine AtonyUterine Atony With HemorrhageElective Cesarean Section

Part of Women’s health & pregnancy clinical trials.

This study compares two ways of giving the medicine oxytocin (which helps the womb tighten to reduce bleeding) after a C-section in women at high risk for heavy bleeding. It will see if giving it as a single injection or as a slow drip works better at preventing excessive blood loss.

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 (not emergency) C-section with spinal or combined spinal-epidural anesthesia.
  • Your doctor has identified you as being at high risk for heavy bleeding after delivery.
  • You have not started labor and your water has not broken before the C-section.
  • You do not have a bleeding disorder, very low platelet count, or take blood thinners that would prevent a spinal block.
  • You do not have placenta accreta (a condition where the placenta grows into the womb wall), severe heart disease, or an allergy to 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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