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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

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

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2000003168
Enrollment
Unknown
Registered
2020-03-31
Start date
2020-04-06
Completion date
Unknown
Last updated
2023-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative nausea and vomiting

Interventions

experimental group:TENS Neiguan (P6) point
control group:No intervention measures

Sponsors

Shanghai Changzheng Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Patients will undergo elective hysteroscopic surgery under general anesthesia; 2. ASA I - II ; 3. Aged 25-50 years.

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
Degree of nausea;Any vomiting or retching;complete response;—

Secondary

MeasureTime frame
Patients' satisfaction with postoperative nausea and vomiting;—

Countries

China

Contacts

Public ContactYonghua Li

Department of Anesthesiology, Shanghai Changzheng Hospital

liyonghua1207@126.com+86 13795439726

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026