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NCT07327866Possibly a fitNot yet recruiting

Comparing two spinal methods to prevent low blood pressure in C-section

Caesarean DeliveryHypotension Postprocedural

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

This trial tests two different spinal anesthesia techniques to see which one better prevents low blood pressure during planned cesarean delivery. It aims to improve safety and comfort for mothers.

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

Phase
Phase 3
Enrollment
94 people
Ages
18 years to 45 years
Study type
Interventional

Who can take part

  • You are a woman between 18 and 45 years old.
  • You are classified as ASA physical status II or III (generally healthy or with mild controlled conditions).
  • You are scheduled for a planned (not emergency) cesarean section under spinal anesthesia.
  • You do not have a known allergy to local anesthetics or any study drugs.
  • You do not have pre-existing high blood pressure requiring medication or pre-eclampsia with severe features.
  • You do not have a serious heart condition that affects blood flow.
  • You do not have a blood clotting disorder, infection at the injection site, or any reason you cannot have spinal anesthesia.
  • You do not have fetal distress or concerning monitoring results.
  • Your body mass index (BMI) is 40 or lower.
  • You are willing to sign an informed consent form.

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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