PONV
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Voluntary participation in this study with signed informed consent; 2.Age 18-65 years, body mass index (BMI) 18-30 kg/m^2, ASA physical status I-III; 3.Apfel risk score of 3 points (i.e., meeting the following three criteria: female gender, history of PONV or motion sickness, non-smoker); 4.Scheduled for painless gastrointestinal endoscopy.
Exclusion criteria
Exclusion criteria: 1.Pregnant or lactating women, or those with pregnancy plans within 3 months; 2.Contraindications or allergic reactions to benzodiazepines or opioid drugs; 3.Previous history of transcutaneous electrical acupoint stimulation, or contraindications to transcutaneous electrical stimulation, including local skin damage or infection at the stimulation site, or presence of implanted electrophysiological devices; 4.Preoperative significant respiratory or circulatory dysfunction, as well as hepatic or renal insufficiency; 5.Communication barriers, including language barriers, history of neurological diseases, or psychiatric disorders; 6.Participation in other clinical trials within the past 3 months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of nausea and vomiting at 24 hours postoperatively;Patient satisfaction score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of nausea and vomiting at 30 minutes and 6 hours postoperatively;Severity of nausea and vomiting at 30 minutes, 6 hours, and 24 hours postoperatively;Quality of recovery from anesthesia at 24 hours postoperatively; | — |
Countries
China
Contacts
The First Affiliated Hospital of Zhengzhou University