About this trial
This study evaluates whether acupuncture at specific body points before and after surgery can improve sleep quality and reduce long-term postoperative pain in patients undergoing video-assisted thoracoscopic lung cancer resection. Eligible adult patients will be randomly assigned to receive either true acupuncture or sham (placebo) acupuncture in addition to standard care. Chronic pain will be assessed during hospital stay and up to 6 months after surgery.
Eligibility criteria
Qualifiers
Patients aged 18-75 years scheduled for elective video-assisted thoracoscopic surgery (VATS) for lung cancer resection.
American Society of Anesthesiologists (ASA) physical status classification I-II.
Body Mass Index (BMI) between 18.5 and 28 kg/m².
Clinical tumor stage according to the 8th edition of the AJCC/UICC TNM Classification: cTis-3N0-1M0.
Disqualifiers
Critical preoperative condition or inability to cooperate.
History of sleep apnea or moderate to severe snoring.
Pittsburgh Sleep Quality Index (PSQI) ≥7 or Athens Insomnia Scale (AIS) score ≥6.
Implanted cardiac pacemaker, preoperative sinus bradycardia (heart rate ≤50 bpm), sinoatrial node disease, or second-/third-degree atrioventricular block.
Trial design
Treatments tested in this trial
- Percutaneous Acupoint Acupuncture
- Sham Acupuncture