Weight loss
Conditions
Interventions
control group:Percutaneous acupoint electrical stimulation to implement false stimulation 3h after surgery, once a day, 30 minutes each time (2 times in 2 days)
Experimental group A:Percutaneous acupoint electrical stimulation to implement true stimulation 3h after surgery, once a day, 30 minutes each time (twice in two days)
Experimental group B:Percutaneous acupoint electrical stimulation at 3h after surgery: true stimulation, once every 12h, for 2 days (3 times in total)
Experimental group C:Percutaneous acupoint electrical stimulation at 3h after surgery: true stimulation, once every 8h, for 2 days (4 times in total)
Sponsors
The First Affiliated Hospital of Chongqing Medical University
Eligibility
Sex/Gender
All
Age
16 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Age >16 years ; 2. Patients who are willing to undergo weight loss surgery and voluntarily sign informed consent; 3. Patients with moderate and high risk PONV risk score; 4. ASA grades II to IV.
Exclusion criteria
Exclusion criteria: 1. Patients who died during the study period; 2. Patients who refuse to participate and do not agree to sign informed consent; 3. Patients with severe mental illness or brain disease injury can not normally complete this survey.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The score of RINVR; | — |
Secondary
| Measure | Time frame |
|---|---|
| PONV risk factor score;The score of EQ-5D-5L;The score of HADS Hospital Anxiety and Depression Scale ;The number of rescues of antiemetic drugs;postoperative complications; | — |
Countries
China
Contacts
Public ContactTang Kailin
Department of Gastrointestinal Surgery, the First Affiliated Hospital of Chongqing Medical Universityyanqing
Outcome results
None listed