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Clinical Trials/ITMCTR2000002891
ITMCTR2000002891
Recruiting
Phase 4

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

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
The First Affiliated Hospital of Xi'an Jiaotong University
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
All

Investigators

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Not specified

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