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PONV Prevention Via Percutaneous Nerve Electrical Stimulation on PC6

Postoperative Nausea and Vomiting Clinical Trial

Official title:
Perioperative Percutaneous Electrical Nerve Stimulation Via a Wearable Equipment on Postoperative Nausea and Vomiting（PONV） in Patients Undergoing Laparoscopy Abdominal Surgery: a Prospective Randomized Controlled Trial

Clinical Trial Summary

This study aims to certify the effectiveness of percutaneous electrical nerve stimulation at Pericardium 6 (PC6) via a wearable equipment during perioperative period on preventing postoperative nausea and vomiting.

Clinical Trial Description

Introduction: This study aims to certify the effectiveness of percutaneous electrical nerve stimulation at Pericardium 6 (PC6) via a wearable equipment during perioperative period on preventing postoperative nausea and vomiting. Method and analysis: A total of approximately 302 patients undergoing elective laparoscopic surgery will be enrolled. Participants will be randomly assigned to either a electrical stimulation group or a placebo group, with computer-generated randomization and concealed allocation using sealed envelopes. The electrical stimulation group will receive PC point electrical stimulation 30 minutes before surgery until 24 hours postoperatively, while the placebo group will wear a wristband without stimulation. The primary outcome will be the incidence of postoperative nausea and vomiting, with secondary outcomes including the incidence of nausea and vomiting within 24 hours after surgery, gastrointestinal and hemodynamic indices, postoperative recovery, hospital stay and cost, and complications. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06241547
Study type Interventional
Source Peking Union Medical College Hospital
Contact Chen Junjie
Phone +8617330860407
Email 1045034956@qq.com
Status Recruiting
Phase Phase 2
Start date January 12, 2024
Completion date December 30, 2024
View Details
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