Accupressure of P6 to Reduce Nausea During Cesarean Section

Status Completed

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

Clinical Trial Details

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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