The Effect of Oliceridine Patient-Controlled Intravenous Analgesia on Postoperative Chronic Pain After Video-Assisted Thoracoscopic Lobectomy

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18-75
SponsorTianjin Medical University General Hospital

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

Treatment groups

320 Participants
are divided into 2 treatment groups

Locations

This trial has no locations