Clin2
NCT07687355Likely a fitNot yet recruiting

Comparing oxytocin delivery methods during cesarean section

Comparing 2 Techniques of iv Oxytocin Causing Hemodynamic Changes

Part of Heart & circulation, Women’s health & pregnancy clinical trials.

This trial compares two ways of giving oxytocin (a medicine that helps the uterus contract) during a cesarean section under spinal anesthesia. It will check how each method affects your blood pressure and heart rate during and after delivery.

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

Phase
N/A
Enrollment
262 people
Ages
18 years to 40 years
Study type
Interventional

Who can take part

  • You must be a woman between 18 and 40 years old.
  • You are scheduled for a cesarean section (C-section) with spinal anesthesia.
  • You will receive oxytocin, a medicine that helps the womb contract after delivery.
  • You cannot have placenta previa (when the placenta covers the cervix).
  • Your water must not have broken before the surgery.
  • You cannot have high blood pressure, diabetes, or be taking immune-suppressing 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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