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Clinical Trials/ITMCTR2000003168
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

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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
Female

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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