chronic postoperative pain
Conditions
Interventions
Sponsors
Eligibility
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
| Measure | Time frame |
|---|---|
| Incidence of chronic pain postoperatively; | — |
Secondary
| Measure | Time 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
Affiliated Hospital of Xuzhou Medical University