ITMCTR2100004254
Recruiting
Phase 1
A randomized controlled study of the effect of percutaneous acupoint electrical stimulation on the incidence of postoperative nausea and vomiting in patients undergoing thoracic surgery
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Shanghai General hospital
- Status
- Recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\) Patients undergoing thoracic surgery under elective general anesthesia;
- •2\) At least 18 years old and below 65 years old;
- •3\) BMI15\-40kg/m2;
- •4\) ASA I \- III level;
- •5\) PONV risk prediction score APFEL \>\= 3 points;
- •6\) Can understand and sign the informed consent, and cooperate with the completion of intervention and assessment.
Exclusion Criteria
- •1\) Pregnancy and lactation;
- •2\) The contraindication of transcutaneous electrical stimulation: the patients with skin allergy, damage, infection, itching, allergy to tape and pacemaker implantation at the test acupoint;
- •3\) A history of alcohol, opioid, or other substance abuse is confirmed/suspected;
- •4\) A history of neurological diseases (cerebral infarction, TIA, Parkinson's disease, mental retardation, craniocerebral injury);
- •5\) Participate in other clinical studies within 3 months before inclusion in this study.
Outcomes
Primary Outcomes
Not specified
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