ITMCTR2000003168
Recruiting
Phase 1
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
ConditionsPostoperative nausea and vomiting
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Postoperative nausea and vomiting
- Sponsor
- Shanghai Changzheng Hospital
- Status
- Recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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.
Outcomes
Primary Outcomes
Not specified
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