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The Effects of Programmed Death-ligand 1 on Postoperative Pain for Lung Cancer Patients

Not yet recruiting
Conditions
Lung Cancer
Postoperative 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
Inclusion Criteria
  1. American Society of Anesthesiologists physical status I-IV (males and females).
  2. 18-80 years of age.
  3. Patients undergoing video-assisted thoracoscopic surgery for malignant lung disease.
Exclusion Criteria
  1. History of opioid abuse.
  2. Known psychiatric disorders.
  3. Unexpected conversion to thoracotomy or transferred to intensive care unit for further treatment.
  4. Combined with other surgeries or sites.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
the incidence of chronic pain after surgery3 months after surgery

Patients were followed up by the Brief Pain Inventory questionnaire about the details of chronic pain.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Peking University People's Hospital

🇨🇳

Beijing, Beijing, China

Peking University People's Hospital
🇨🇳Beijing, Beijing, China
Yi Feng, MD
Contact

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