postoperative pain
Conditions
Interventions
Sponsors
The First Hospital Of Jiaxing
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Aged >= 18 years, gender not limited; 2. ASA classification I-III; 3. Proposed elective unilateral thoracoscopic surgery; 4. Voluntarily participate in this study and sign an informed consent form.
Exclusion criteria
Exclusion criteria: 1. Contraindications for rTMS (such as intracranial metal implants, pacemakers, personal or family history of epilepsy); 2. Long-term use of opioids, sedative medications, or a diagnosis of chronic pain syndrome; 3. Severe mental or cognitive dysfunction that prevents them from communicating or cooperating with the assessment; 4. History of drug or alcohol abuse; 5. Pre-operative pre-existing neurological deficits; 6. Pregnant or breastfeeding women; 7. Any other circumstances that the researcher considers unsuitable for participation in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of moderate to severe pain at 24 hours postoperatively; | — |
Secondary
| Measure | Time frame |
|---|---|
| Time to first postoperative self-controlled analgesia;Postoperative resting pain score;Length of stay in resuscitation room;Area under the resting pain intensity curve at 48 hours postoperatively;Postoperative motor pain scores;Postoperative recovery quality index;Extraction time;Area under the exercise pain intensity curve at 48 hours postoperatively;Remedial analgesic dosage (morphine mg equivalent) in the first 48 hours postoperatively; | — |
Countries
China
Contacts
Public ContactNi Huadong
The First Hospital of Jiaxing
Outcome results
None listed