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Effects of transcutaneous vagus nerve stimulation on postoperative gastrointestinal function in elderly patients after spinal surgery

Effects of transcutaneous vagus nerve stimulation on postoperative gastrointestinal function in elderly patients after spinal surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110876
Enrollment
Unknown
Registered
2025-10-22
Start date
2024-07-23
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Postoperative gastrointestinal dysfunction

Interventions

Intervention Group:The vagus nerve electrical stimulation pattern is set to a sparse wave, with a frequency of 20 Hz and an electrical current intensity of 30mA. The electrodes are placed in the tragu
Control group:Transcutaneous vagal nerve stimulation was not performed at the beginning of the procedure.

Sponsors

The Fourth Hospital of Wuhan
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. ASA I ~ III grade; 2. Age 60-80 years old, gender not limited; 3. Body mass index of 18 ~ 28kg/m^2; 4. The estimated duration of the surgery is 2-4 hours; 5. Patients who have not used any gastrointestinal motility promoting drugs before surgery and have normal gastrointestinal function; 6. Agree to use postoperative analgesia; 7. Patients who can understand the experimental content and cooperate; 8. Patients and their families undergo the experiment and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of abdominal or gastrointestinal surgery; 2. Patients with a history of ear surgery or ear skin infection; 3. Patients with diabetes or severe cerebrovascular disease; 4. Patients with spinal tumors, infections, or deformities; 5. Patients with obvious preoperative hypokalemia, hypoproteinemia, or anemia; 6. Patients with long-term preoperative fasting and drinking prohibition; 7. Patients with a history of ventilatory difficulties or delayed extubation; 8. Patients with sinus bradycardia, prolonged PR interval, or atrioventricular block.

Design outcomes

Primary

MeasureTime frame
First postoperative exhaust time;Time of first postoperative defecation;Postoperative bowel sound recovery;Postoperative abdominal distension;

Secondary

MeasureTime frame
VAS scores;Cholecystokinin;Patient satisfaction 1 day after surgery;Length of stay;

Countries

China

Contacts

Public ContactCheng Jiangxia

The Fourth Hospital of Wuhan

425878218@qq.com+86 136 2453 6268

Outcome results

None listed

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