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Electroencephalogram Changes Induced by Transcutaneous Electrical Acupoint Stimulation

RecruitingNAAges 18 Years - 80 YearsAllBeijing Chao Yang Hospital
NCT07819630 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

A total of 90 subjects underwent abdominal surgery under general anesthesia at Chaoyang Hospital in Beijing. The subjects were divided into a percutaneous acupoint electrical stimulation group and a control group. The subjects were selected for TEAS stimulation at the Neiguan, Hegu, and Zusanli acupoints on both sides, and EEG data were collected using a 32 lead EEG cap test throughout the entire process. During the experiment, changes in hemodynamic parameters (blood pressure, heart rate) and perioperative pain scores of the subjects will be recorded.

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📋 Eligibility rules (as published)
Inclusion Criteria:1. Age between 18 and 80 years; 2. ASA physical status classification I-II; 3. Scheduled to undergo abdominal surgery under general anesthesia (e.g., gastrectomy, colorectal cancer surgery, etc.); 4. Consent to participate in the study and signing of the informed consent form. \- Exclusion Criteria:1. Impaired cognitive function or language communication disorders; 2. Mental disorders, epilepsy, or abnormal EEG activity; 3. Receipt of acupoint therapy within two weeks prior to surgery; 4. Presence of a cardiac pacemaker or metal implants; 5. Allergy to surface electrodes; 6. Concomitant medical conditions (e.g., dermatological disorders) that may affect treatment or trial administration. \-
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What it tests

  • Transcutaneous electrical acupoint stimulation
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Where

1 site
Affiliated Beijing Chaoyang Hospital of Capital Medical University, Beijing 100020
Beijing, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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