A clinical study of transcutaneous acupoint electrical stimulation combined with electroacupuncture to promote rapid recovery of patients after open abdominal surgery in gastrointestinal surgery
- Conditions
- Postoperative gastrointestinal dysfunction
- Registration Number
- ITMCTR2100004766
- 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
1. Aged 18 - 70 years, gender is not limited;
2. Resection of gastric or colorectal tumors under general anesthesia;
3. Voluntary participation in this study and signed informed consent.
1. The surgical incision passes through the abdominal acupoints selected in this study;
2. The selected acupoints have local skin infections;
3. Patients who cannot understand or cooperate with assessments such as VAS scores;
4. Patients who are allergic to metals or severely afraid of acupuncture, and cannot tolerate transcutaneous electrical acupoint stimulation or electroacupuncture;
5. Patients with uncontrolled diabetes, severe heart, central nervous system, mental illness or blood coagulation dysfunction;
6. Patients with a pacemaker;
7. Patients who are participating in other research trials.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time of first postoperative bowel movement;Time that the patients tolerated a solid diet;
- Secondary Outcome Measures
Name Time Method Postoperative daily pain visual analog scale scores and analgesic use;Hospital days from surgery to discharge from rehabilitation for patients;Time to first ambulation after surgery;Time to first flatus after operation;Incidence of postoperative complications;Acceptability evaluation of each type of acupuncture at the end of treatment;Incidence, degree of postoperative daily nausea and vomiting vas and antiemetic use;