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Efficacy of simultaneous combining of transcranial direct current stimulation and transcutaneous auricular vagus nerve stimulation on the prevention of chronic postoperative pain after video-assisted thoracoscopic lung surgery

Efficacy of simultaneous combining of transcranial direct current stimulation and transcutaneous auricular vagus nerve stimulation on the prevention of chronic postoperative pain after video-assisted thoracoscopic lung surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085471
Enrollment
Unknown
Registered
2024-06-07
Start date
2024-06-15
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

chronic postoperative pain

Interventions

sham group:The electrodes of the instrument are placed in the corresponding position, but no stimulation is given.
tDCS group:The transcranial direct current stimulation is performed. The left dorsolateral prefrontal lobe is stimulated by the anode, and the right supraorbital is stimulated by the cathode. The stim
taVNS group:The transcutaneous auricular vagus nerve stimulation is performed. The cymba conchae of the patients left ear is stimulated with a pulse width of 200 um, a frequency of 25 Hz, and a stimul
SJS group:The transcranial direct current stimulation and transcutaneous auricular vagus nerve stimulation are performed at the same time. The electrodes of the instrument are placed in the correspond

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Age 18 to 75 years; initial diagnosis allows for direct video-assisted thoracoscopic lung surgery; American Society of Anesthesiologists physical status classification I to III; Anesthesia by combined intravenous-inhalation anesthesia

Exclusion criteria

Exclusion criteria: Refusal to sign the trial consent form; Already participating in another interventional study; Neuropsychiatric disorders or a previous history of neurological or psychiatric disorders; Cranial or scalp injuries; Visual and hearing impairments as well as difficulty in communicating; Refusal to use an analgesic pump; Damage or inflammation of the skin of the ear cavities, such as in case of ear disorders (e.g., tympanic membrane perforation, etc.); Metallic implantation in the body or fitting of cochlear implants; Abnormal preoperative electrocardiograms; Substance or alcohol abuse; allergy to relevant medications in the trial protocol

Design outcomes

Primary

MeasureTime frame
Incidence of chronic pain postoperatively;

Secondary

MeasureTime frame
Postoperative pain level score;Postoperative analgesic drug use;Adverse event;Postoperative complication;Postoperative cough score;Postoperative nausea and vomiting score;Postoperative anxiety and depression scores;Brain fMRI;

Countries

China

Contacts

Public ContactJun-Li Cao

Affiliated Hospital of Xuzhou Medical University

caojl0310@aliyun.com+86 151 6216 0809

Outcome results

None listed

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