postoperative recovery quality
Conditions
Interventions
Control group:Sham stimulation
Sponsors
Army Medical Center of PLA
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Age: greater than 18 years old; 2. ASA classification: I-III; 3. Type of surgery: patients scheduled for elective thoracoscopic lung surgery; 4. Informed consent: patients voluntarily participate and sign written informed consent.
Exclusion criteria
Exclusion criteria: 1. Presence of intracranial metal implants, cardiac pacemaker, implantable cardioverter-defibrillator (ICD), or cochlear implant; Personal or family history of epilepsy; 2. History of neurological or psychiatric disorders; 3. Severe hearing, visual, speech, or cognitive impairment that, in the investigator's judgment, precludes cooperation with TMS treatment and postoperative follow-up assessments; 4. Clear history of drug or alcohol abuse; 5. Pre-existing history of chronic pain with long-term regular use of opioid analgesics; 6. Concurrent severe cardiac, hepatic, or renal dysfunction.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative 24-hour Recovery Quality; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative pulmonary complications;Postoperative sleep quality;Postoperative 48-hour Recovery Quality;postoperative pain;Postoperative anxiety and depressive symptoms; | — |
Countries
China
Contacts
Public ContactQingxiang Mao
Army Medical Center of PLA
Outcome results
None listed