The Effects of Programmed Death-ligand 1 on Postoperative Pain for Lung Cancer Patients
1 other identifier
observational
100
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jul 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 26, 2024
CompletedFirst Posted
Study publicly available on registry
July 16, 2024
CompletedStudy Start
First participant enrolled
July 20, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2025
CompletedSeptember 19, 2024
June 1, 2024
7 months
June 26, 2024
September 10, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
the incidence of chronic pain after surgery
Patients were followed up by the Brief Pain Inventory questionnaire about the details of chronic pain.
3 months after surgery
Study Arms (2)
high expression of programmed death-ligand 1
According to the distribution of PD-L1 concentration levels in the plasma, participants were divided into two groups: high expression of PD-L1 (PD-L1(H)) and low expression of PD-L1 (PD-L1(L)).
low expression of programmed death-ligand 1
According to the distribution of PD-L1 concentration levels in the plasma, participants were divided into two groups: high expression of PD-L1 (PD-L1(H)) and low expression of PD-L1 (PD-L1(L)).
Eligibility Criteria
Patients underwent video-assisted thoracoscopic surgery for malignant lung disease.
You may qualify if:
- American Society of Anesthesiologists physical status I-IV (males and females).
- years of age.
- Patients undergoing video-assisted thoracoscopic surgery for malignant lung disease.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Peking University People's Hospital
Beijing, Beijing Municipality, 100037, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Xue Tian, MD
Peking University People's Hospital
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- director of department of Anesthesiology and Pain medicine
Study Record Dates
First Submitted
June 26, 2024
First Posted
July 16, 2024
Study Start
July 20, 2024
Primary Completion
February 1, 2025
Study Completion
March 1, 2025
Last Updated
September 19, 2024
Record last verified: 2024-06