Clin2
NCT05488457Possibly a fitRecruiting

Oxytocin timing and effects during planned C-section

Post Partum HemorrhageCesarean Section ComplicationsBlood Loss

Part of Women’s health & pregnancy clinical trials.

This study looks at how oxytocin (a medicine often used to help with labor and uterine contractions) moves through the body and what it does during a non-emergency C-section. It may help improve how oxytocin is used in the future for safer, more predictable delivery care.

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

Phase
Phase 2
Enrollment
100 people
Ages
18 years to 50 years
Study type
Interventional

Who can take part

  • You are between 18 and 50 years old
  • You are currently pregnant and the baby is developing inside the uterus
  • You are at term pregnancy (over 39 weeks, or 37–39 weeks if there’s a medical reason to deliver)
  • You are having a C-section that is not an emergency (planned or done because of a non-urgent situation)
  • You do not have an allergy or known reason you can’t take oxytocin
  • You can understand the study and sign informed consent

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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