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Effect of percutaneous acupoint electrical stimulation on perioperative anxiety in patients undergoing laparoscopic sleeve gastrectomy

Effect of percutaneous acupoint electrical stimulation on perioperative anxiety in patients undergoing laparoscopic sleeve gastrectomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093495
Enrollment
Unknown
Registered
2024-12-05
Start date
2024-07-04
Completion date
Unknown
Last updated
2024-12-09

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: Gender is not limited, age: 18-50 years old patients who are informed and voluntarily participate in this study and sign informed consent forms, ASA II-III level, 30kg/m^2<= BMI <=45kg/m^2, elective general anesthesia for laparoscopic sleeve gastrectomy.

Exclusion criteria

Exclusion criteria: The contraindications for transcutaneous electrical stimulation include local skin breakage infection and the presence of implanted electro-physiological devices in the body. It is also contraindicated in individuals with a history of severe cardiovascular or cerebrovascular diseases abnormal liver or kidney function or endocrine disorders. Additionally it is not recommended for those who are on long-term use of psychiatric medications or have a history of alcohol abuse or illicit drug use. Other conditions that are considered unsuitable for this treatment are also included.

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