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Clinical Trials/ITMCTR2100004517
ITMCTR2100004517
Recruiting
Phase 1

A clinical study of Transcutaneous electrical acupoint stimulation (TEAS) combined with electroacupuncture (EA) to promote rapid recovery after abdominal surgery

West China Hospital, Sichuan University0 sitesTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
West China Hospital, Sichuan University
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
All

Investigators

Sponsor
West China Hospital, Sichuan University

Eligibility Criteria

Inclusion Criteria

  • 1\. Age 18 \- 70 years, sex not restricted;
  • 2\. Resection of hepatobiliary, gastrointestinal, renal, or bladder tumors was performed under general anesthesia;
  • 3\. Voluntary participation in this study and signed informed consent.

Exclusion Criteria

  • 1\. The surgical incision was made through the abdominal acupoints selected for this study;
  • 2\. The selected acupoints had local skin infection;
  • 3\. Patients who could not understand or cooperate with assessments such as VAS scores;
  • 4\. Those with hypersensitivity to metals or severe fear of acupuncture, transcutaneous electrical acupoint stimulation, or intolerance to electroacupuncture treatment;
  • 5\. Patients with uncontrolled diabetes, severe cardiac, central nervous, psychiatric disorders, or coagulopathy;
  • 6\. Placement of pacemaker;
  • 7\. Patients being enrolled in other research trials.

Outcomes

Primary Outcomes

Not specified

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