Clinical study on the prevention and treatment of nausea and vomiting after general anesthesia with domestic wearable transcutaneous acupoint electric stimulation bracelet: a prospective randomized trial
Phase 1
Recruiting
- Conditions
- Postoperative nausea and vomiting
- Registration Number
- ITMCTR2000003168
- Lead Sponsor
- Shanghai Changzheng Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
1. Patients will undergo elective hysteroscopic surgery under general anesthesia;
2. ASA I - II ;
3. Aged 25-50 years.
Exclusion Criteria
1. Patients with nausea, vomiting and taking antiemetic drugs 24 hours before surgery;
2. Pregnant and lactating women;
3. Patients with abnormal heart, lung, liver and kidney function;
4. Patients who refuse bracelet treatment.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Degree of nausea;Any vomiting or retching;complete response;
- Secondary Outcome Measures
Name Time Method Patients' satisfaction with postoperative nausea and vomiting;