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

Phase 1
Recruiting
Conditions
Postoperative gastrointestinal dysfunction
Registration Number
ITMCTR2100004517
Lead Sponsor
West China Hospital, Sichuan University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
Not specified
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.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time to first postoperative flatus;
Secondary Outcome Measures
NameTimeMethod
pain and Nausea Vomiting scores on visual analogue scale (from 0 which implied no at all, to 10 which implied the worst)and medication use;Incidence of postoperative complications;hospital days from operation to discharge;Time of first postoperative anal spontaneous defecation; Time to first ambulation;acceptability assessment of treatment;time that the patients tolerated a solid diet;
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