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Clinical Trials/ITMCTR2100004254
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.

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

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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