Transcutaneous Electrical Acupoint Stimulation for Prevention of Postoperative Nausea and Vomiting: a Multicenter, Evaluator-Blind, Randomized and Controlled Trial

Phase 4

Recruiting

• Conditions: on-gastrointestinal laparoscopic surgery

• Registration Number: ITMCTR2000002891
• Lead Sponsor: The First Affiliated Hospital of Xi'an Jiaotong University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

1. Patients for selective laparoscopic non-gastrointestinal surgery under general anesthesia;
2. Aged 18–50 year, BMI 15-40 kg/m2, ASA,class I-III;
3. Apfel's score of PONV risk prediction >=3 points;
4. Ability to understand, sign informed consent and cooperate with the intervention and evaluation.

Exclusion Criteria

1. Pregnancy and breast feeding women
2. TEAS contraindications: skin allergy, breakage, infection or itching of test points, allergy toadhesive tape,
pacemaker implant;
3. Confirmation/suspection a history of alcohol, opioid or other drugs;
4. Admission to ICU after surgery;
5. Participation in other clinical studies within 3 months before admission to this study.

Study & Design

• Study Type: Interventional study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Incidence of first Index of PONV;

Secondary Outcome Measures

Name	Time	Method
ausea;Vomiting;