ITMCTR2000002891RecruitingPhase 4
Transcutaneous Electrical Acupoint Stimulation for Prevention of Postoperative Nausea and Vomiting: a Multicenter, Evaluator-Blind, Randomized and Controlled Trial
Trial Snapshot
- Phase
- Phase 4
- Status
- Recruiting
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional study
Eligibility Criteria
- Ages
- 18 to 50 (—)
- Sex
- All
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.
Investigators
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