Non-gastrointestinal laparoscopic surgery
Conditions
Interventions
Experimental group:Transcutaneous Electrical Acupoint Stimulation
Sponsors
The First Affiliated Hospital of Xi'an Jiaotong University
Eligibility
Sex/Gender
All
Age
18 Years to 50 Years
Inclusion 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
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of first Index of PONV; | — |
Secondary
| Measure | Time frame |
|---|---|
| Vomiting;Nausea; | — |
Countries
China
Contacts
Public ContactJie Fang
The First Affiliated Hospital of He'nan University of Chinese Medicine
Outcome results
None listed