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A clinical observational study on the effect of percutaneous acupoint electrical stimulation on stress response in patients undergoing unilateral dual-channel spinal endoscopic surgery.

A clinical observational study on the effect of percutaneous acupoint electrical stimulation on the stress response in patients undergoing spinal UBE surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000072
Enrollment
Unknown
Registered
2026-01-13
Start date
2024-09-01
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Lumbar degenerative disease

Interventions

Total intravenous anesthesia group:Only electrode pads are connected
no electrical stimulation is administered.
Acupuncture-assisted anesthesia continuous wave group:the TEAS device uses 100Hz continuous wave stimulation
Acupuncture-assisted anesthesia sparse-dense wave group:the TEAS device uses 2/100Hz sparse-dense wave stimulation

Sponsors

Hangzhou Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age 40–70 years, American Society of Anesthesiologists (ASA) classification I or II; 2. Imaging diagnosis indicating indications for unilateral dual-channel spinal endoscopic surgery, including herniated disc (without ruptured annulus fibrosus), lumbar spinal stenosis, vertebral spondylolisthesis, etc.; 3. No contraindications to medications used in this study; 4. No history of nerve injury or surgery at acupoints (Zusanli, Sanyinjiao); 5. Patients provide written informed consent and agree to cooperate in completing the entire study and follow-up.

Exclusion criteria

Exclusion criteria: 1. Comorbid immune system diseases; 2. Infectious disease within the past week; 3. Diabetes mellitus with poor glycemic control (fasting blood glucose =8.0 mmol/L or/and 2-hour postprandial blood glucose =10.0 mmol/L); 4. Body mass index =30 kg/m²; 5. Use of high-dose glucocorticoids within 2 days prior to surgery; 6. Poor nutritional status, plasma albumin concentration <35 g/L, serum total protein concentration <60 g/L; 7. Comorbid malignancy, severe cardiovascular disease (such as heart failure, severe arrhythmia, etc.); 8. Mental disorders, cognitive impairment, or other reasons preventing cooperation in this study.

Design outcomes

Primary

MeasureTime frame
Stress response indicators;

Secondary

MeasureTime frame
Intraoperative hemodynamic parameters;Perioperative duration;Postoperative pain and sedation score;Postoperative complication rate;

Countries

China

Contacts

Public ContactLi Yanan

Hangzhou Hospital of Traditional Chinese Medicine

15306505390@163.com13588363487

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 7, 2026