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

Status: Recruiting
Location: See location...
Intervention Type: Device, Drug
Study Type: Interventional
Study Phase: Phase 2
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: t
View:

• Patients aged 18-65 years;

• Patients undergoing elective laparoscopic surgery;

• American Society of Anaesthesiologists(ASA) Grade 1 to 3;

• Anesthesia: General Anesthesia, Tracheal Intubation;

• BMI: ≥18, \<28;

• Gender: female

• Patients or their family members are able to comprehend the study protocol and are willing to participate in this research by providing written informed consent.

Locations
Other Locations
China
Peking Union Medical College Hospital
RECRUITING
Beijing
Contact Information
Primary
Chen Junjie
1045034956@qq.com
+8617330860407
Time Frame
Start Date: 2024-01-12
Estimated Completion Date: 2024-12-30
Participants
Target number of participants: 302
Treatments
Experimental: stimulation group
accept general drug prevention, wear the equipment, and receive electrical stimulation.
Placebo_comparator: control group
accept general drug prevention and wear the equipment but receive no electrical stimulation
Related Therapeutic Areas
Sponsors
Leads: Peking Union Medical College Hospital

This content was sourced from clinicaltrials.gov