Clin2
NCT05233462Possibly a fitRecruiting

Compare two spinal anesthesia bupivacaine dose methods for C-sections

Regional Anesthesia MorbidityCesarean Section ComplicationsLocal Anesthetic Complication

Part of Women’s health & pregnancy clinical trials.

This trial looks at whether adjusting the dose of bupivacaine by height works better than using a standard dose for spinal anesthesia during planned C-sections. It may help improve safety and comfort by aiming for the right level of numbing effect.

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

Phase
N/A
Enrollment
250 people
Ages
18 years to 45 years
Study type
Interventional

Who can take part

  • Your C-section must be planned (not an emergency)
  • You must be pregnant at term: more than 35 weeks
  • You need to agree to join the study by signing consent forms
  • You must be able to receive spinal (intrathecal) anesthesia
  • You should not have certain medical conditions that affect spinal anesthesia safety

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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