With this research the investigators hope to determine the lowest dose of ropivacaine used in
transversus abdominis plane (TAP) blocks that can effectively treat pain in women after
cesarean section (c-section).
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Full eligibility criteria for NCT02893423
Ages eligible for Study
Genders eligible for Study
Accepts Healthy Volunteers
Pregnant patients undergoing elective c-section
Allergy to local anesthetics
Contraindication to tap blocks
All locations for NCT02893423
United States (1)
Maimonides Medical Center
Brooklyn, New York, United States, 11219
View full eligibility
Tris trial is registered with FDA with number: NCT02893423. The sponsor of the trial is Maimonides Medical Center and it is looking for 51 volunteers for the current phase.
Official trial title: The Dose Dependent Effect of Ropivacaine Transversus Abdominis Plane Blocks on Postoperative Analgesia After Cesarean Section
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