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Effects of transcutaneous electrical acupoint stimulation on perioperative anxiety and quality of recovery in obese patients undergoing laparoscopic bariatric surgery

Effects of transcutaneous electrical acupoint stimulation on perioperative anxiety and quality of recovery in obese patients undergoing laparoscopic bariatric surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098328
Enrollment
Unknown
Registered
2025-03-06
Start date
2025-03-08
Completion date
Unknown
Last updated
2025-03-10

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

Conditions

Anxiety

Interventions

Sponsors

Jiangsu Provincial People's Hospital Suqian Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Gender is not limited; 2. Age: Patients aged 18~60 years old are informed and voluntarily participate in this study, and have signed the informed consent form; 3. ASA Class II-III; 4.30kg/m^2<=BMI <=45kg/m^2; 5. Elective general anesthesia for laparoscopic sleeve gastrectomy.

Exclusion criteria

Exclusion criteria: 1. Patients with contraindications to percutaneous electrical stimulation: including local skin ulceration, infection and implantation of internal electrophysiological devices, history of severe cardiovascular and cerebrovascular diseases, abnormal liver and kidney function or endocrine disorders before surgery; 2. Long-term use of psychotropic drugs or abuse of alcohol or illegal drugs; 3. Have a history of allergies, chronic pain, and psychiatric illness, in addition, including other conditions that are considered difficult to include.

Design outcomes

Primary

MeasureTime frame
Rate of anxiety discovery;

Secondary

MeasureTime frame
Postoperative 1d, 2d, 3d VAS visual analog scale scores for rest and activity, pain percentage, and number of times the postoperative analgesia pump was pressed and the number of rescue analgesia cases;The incidence of postoperative nausea and vomiting (PONV) on days 1, 2, and 3, and the number of prescribed antiemetic medications used;Record the patient's general information, including gender, age, education level, surgical history, Body Mass Index (BMI), and ASA classification.;The use of propofol and remifentanil during surgery, surgery time (the duration from skin incision to skin suture completion), extubation time, and discharge time from the recovery room.;

Countries

China

Contacts

Public ContactQiannan Fan

Jiangsu Provincial People's Hospital Suqian Hospital

584595226@qq.com+86 152 6120 6830

Outcome results

None listed

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