Clin2
NCT07853482Possibly a fitNot yet recruiting

Comparing two pain blocks after planned cesarean delivery

Postoperative Pain After Cesarean Section

Treatments studied

Part of Pain clinical trials.

This study tests two different numbing injections (nerve blocks) after a planned cesarean delivery to see which one controls pain better. If you qualify, you'll receive one of the two blocks to help you recover with less pain after birth.

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

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

Who can take part

  • You are between 18 and 40 years old.
  • Your cesarean delivery is planned (not emergency) and you are between 37 and 41 weeks pregnant.
  • You are expecting only one baby (not twins, triplets, etc.).
  • You do not have allergies to local numbing medicines (like ropivacaine or bupivacaine) or to nonsteroidal anti-inflammatory drugs (like ketoprofen).
  • You do not have chronic pain or take strong painkillers (opioids) regularly before surgery.
  • You do not have pre-eclampsia, and your body mass index (BMI) is 35 or lower.

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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