🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in China / NCT06957912
Recruiting Not applicable

Transcutaneous Auricular Vagus Nerve Stimulation and Quality of Recovery After Major Noncardiac Surgery

NCT06957912 · tracked via the Priya Life Science China tracker
Sponsor
Peking University First Hospital
Phase
Not applicable
Started
2025-05-13
Last updated
2025-06-03

Condition(s) studied

Vagus Nerve StimulationTranscutaneous Electric Nerve StimulationNoncardiac SurgeryQuality of Recovery

Investigational drug(s) / intervention(s)

Transcutaneous auricular vagus nerve stimulationSham stimulation

Transcutaneous auricular vagus nerve stimulation: Transcutaneous auricular vagus nerve stimulation is performed using earphone-shaped stimulators (tVNS501, Ruishenan Medical Device, Inc. JiangSu, China) on the left tragus areas of the outer ear for a total of 30 min. Using parameters we have identified through systematic review, electrical stimulation (pulse width: 200-300 μs; frequency: 25 Hz; duty cycles: 50%) is initiated at 200% perceptual threshold (PT) which means the minimum amount of electricity required to perceive electrical stimulation on the skin described as a pricking or tingling sensation. All conscious patients will be told they may or may not feel any sensation from the stimulation. The stimulation will be performed between 15:00 and 17:00 on the first day before surgery, at least 30 minutes before the start of surgery and between 08:00 and 10:00 on the first to third day after surgery.

Sham stimulation: Sham stimulation is performed using earphone-shaped stimulators (tVNS501, Ruishenan Medical Device, Inc. JiangSu, China) on the left tragus areas of the outer ear for a total of 30 min. Using parameters we have identified through systematic review, electrical stimulation (pulse width: 200-300 μs; frequency: 25 Hz; duty cycles: 50%) is initiated at 200% perceptual threshold (PT) which means the minimum amount of electricity required to perceive electrical stimulation on the skin described as a pricking or tingling sensation. And the current will be automatically switched off after 15 s. All conscious patients will be told they may or may not feel any sensation from the stimulation. The stimulation will be performed between 15:00 and 17:00 on the first day before surgery, at least 30 minutes before the start of surgery and between 08:00 and 10:00 on the first to third day after surgery.

Study summary

Transcutaneous auricular vagus nerve stimulation (taVNS) is a novel non-invasive neuromodulation technique. Existing evidence suggested that taVNS improves pain management, sleep quality, inflammatory responses, and gastrointestinal recovery after surgery. This study is designed to test the hypothesis that perioperative use of taVNS may improve quality of recovery in patients after major noncardiac surgery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
85 Years
Healthy volunteers
No
Inclusion Criteria: 1. Aged ≥18 years but \<85 years. 2. Scheduled for elective or limited-time noncardiac surgery with expected duration ≥2 hours. Exclusion Criteria: 1. Lesions or infections of the auricle skin. 2. Recent or long-term use of cholinergic or anticholinergic medications. 3. Neurosurgery. 4. Expected mechanical ventilation with intubation for ≥1 day after surgery. 5. Diagnosed schizophrenia, epilepsy, Parkinson's disease, or myasthenia gravis before surgery. 6. Preoperative left ventricular ejection fraction (LVEF) \<30%, or those with sick sinus syndrome, sinus bradycardia (heart rate \<50 beats per minute), atrioventricular block of grade II or above, or implanted pacemaker. 7. Inability to communicate due to coma, severe dementia, or language barrier before surgery, or unable to cooperate with intervention. 8. American Society of Anesthesiologists physical status grade \>IV, or estimated survival \<24 hours.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Peking University First Hospital Beijing Beijing Municipality Recruiting

More Peking University First Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06957912 on ClinicalTrials.gov ↗ ← All trials in China