NCT06503432

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

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jul 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 26, 2024

Completed
20 days until next milestone

First Posted

Study publicly available on registry

July 16, 2024

Completed
4 days until next milestone

Study Start

First participant enrolled

July 20, 2024

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2025

Completed
28 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2025

Completed
Last Updated

September 19, 2024

Status Verified

June 1, 2024

Enrollment Period

7 months

First QC Date

June 26, 2024

Last Update Submit

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

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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

RECRUITING

MeSH Terms

Conditions

Lung NeoplasmsPain, Postoperative

Condition Hierarchy (Ancestors)

Respiratory Tract NeoplasmsThoracic NeoplasmsNeoplasms by SiteNeoplasmsLung DiseasesRespiratory Tract DiseasesPostoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Study Officials

  • Xue Tian, MD

    Peking University People's Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Xue Tian, MD

CONTACT

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

Locations