The Effects of Programmed Death-ligand 1 on Postoperative Pain for Lung Cancer Patients
- Conditions
- Lung CancerPostoperative Pain
- Registration Number
- NCT06503432
- Lead Sponsor
- Peking University People's Hospital
- Brief Summary
The concentration of plasma programmed death-ligand 1(PD-L1) for lung cancer patients before video-assisted thoracoscopic surgery is detected. According to the distribution of plasma concentration, patients are divided into high or low expression of PD-L1. Differences in acute and chronic postoperative pain are compared between two groups of patients. And effects of PD-L1 expresion on postoperative pain in lung cancer patients are explained.
- Detailed Description
Chronic pain after video-assisted thoracoscopic surgery (VATS) has been a major concern for lung cancer patients. The relationship between plasma programmed cell death ligand-1 (PD-L1) concentration and chronic pain in post-VATS is uncertain. This study aims to explore the effects of PD-L1 levels on chronic pain and provide proactive pain management regimen according to individual genetic differences.
The concentration of plasma PD-L1 for lung cancer patients before video-assisted thoracoscopic surgery is detected. According to the distribution of plasma concentration, patients are divided into high or low expression of PD-L1. Differences in acute and chronic postoperative pain are compared between two groups of patients. And effects of PD-L1 expresion on postoperative pain in lung cancer patients are explained.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 100
- American Society of Anesthesiologists physical status I-IV (males and females).
- 18-80 years of age.
- Patients undergoing video-assisted thoracoscopic surgery for malignant lung disease.
- History of opioid abuse.
- Known psychiatric disorders.
- Unexpected conversion to thoracotomy or transferred to intensive care unit for further treatment.
- Combined with other surgeries or sites.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the incidence of chronic pain after surgery 3 months after surgery Patients were followed up by the Brief Pain Inventory questionnaire about the details of chronic pain.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Peking University People's Hospital
🇨🇳Beijing, Beijing, China
Peking University People's Hospital🇨🇳Beijing, Beijing, ChinaYi Feng, MDContact
