Postoperative Nausea and Vomiting
Conditions
Interventions
Intervention group:The intervention group will, after entering the operating room on the day of surgery, in addition to undergoing routine monitoring (such as heart rate, blood pressure, oxygen satura
Control group:In this study, patients in the control group will, after entering the operating room on the day of surgery, undergo routine monitoring (including heart rate, blood pressure, oxygen satur
Sponsors
Affiliated Hospital of Jiangsu University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1.Patients with ASA physical status classification of I–II; 2.Patients with no history of anesthesia within the past year; 3.Patients who have not used antiemetic drugs within 1 month before surgery; 4.Patients aged 18–65 years; 5.Patients without severe cardiovascular disease, diabetes, or liver and kidney disease; 6.Patients without psychiatric abnormalities or language communication barriers.
Exclusion criteria
Exclusion criteria: 1.Patients with a cardiac pacemaker; 2.Patients who are afraid of transcutaneous electrical acupoint stimulation (TEAS) and cannot cooperate with the procedure; 3.Patients with skin allergies, damage, or infections at the site of stimulation; 4.Patients who have had a cold within the past week; 5.Patients who have used nonsteroidal anti-inflammatory drugs (NSAIDs), opioids, or corticosteroids within the past month.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of Postoperative Nausea and Vomiting;Duration of Postoperative Nausea and Vomiting;Usage of Antiemetic Drugs;Patient Satisfaction; | — |
Secondary
| Measure | Time frame |
|---|---|
| Time to Relief of Postoperative Nausea and Vomiting; | — |
Countries
China
Contacts
Public ContactWang Yiting
Affiliated Hospital of Jiangsu University
Outcome results
None listed