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Clinical Trial Summary

The purpose of this study is to evaluate if the addition of P6 pressure point stimulation as opposed to sham-point stimulation will decrease intraoperative and postoperative nausea and vomiting (IONV and PONV) for patients undergoing non-emergent cesarean delivery. We hypothesize that the addition of stimulation of the P6 pressure point to our institutional current standard of care (phenylephrine infusion, intravenous fluid bolus, and as needed intraoperative ondansetron) will decrease the occurrence of intraoperative emesis.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04799587
Study type Interventional
Source Northwestern University
Contact
Status Completed
Phase N/A
Start date May 26, 2021
Completion date September 30, 2023

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