About this trial
The primary objective is to evaluate the impact of oliceridine versus sufentanil for perioperative analgesia on the incidence of chronic postsurgical pain (CPSP) in patients undergoing video-assisted thoracoscopic surgery.
Eligibility criteria
Qualifiers
① Age 18-75 years, ASA physical status I-III, BMI 18-30 kg/m²;
Scheduled for unilateral video-assisted thoracoscopic surgery (VATS) lung resection, including wedge resection, segmentectomy, lobectomy, or radical resection for lung cancer;
Preoperative pain score <1 on the Numeric Rating Scale (NRS);
Ability to understand the study objectives and procedures, with voluntary informed consent obtained;
Disqualifiers
① History of chronic pain or long-term analgesic use prior to surgery;
Previous ipsilateral thoracic surgery;
Prior neoadjuvant radiotherapy or chemotherapy;
Severe cardiovascular or cerebrovascular disease, or hepatic/renal dysfunction (ALT/AST >3× upper limit of normal; eGFR <60 mL/min/1.73m²);
Trial design
Treatments tested in this trial
- Oliceridine
- Sufentanil