ClinicalTrials.Veeva

Menu

Establishing a Longitudinal Cohort Study of Lung Cancer Using Tissue and Peripheral Blood Metabolomics.

G

Guangzhou Medical University

Status

Enrolling

Conditions

Metabolomics
Lung Cancer
Lung Cancer (NSCLC)
Lung

Treatments

Other: Monitoring serum metabolites in lung cancer patients using tissue and peripheral blood samples.

Study type

Observational

Funder types

Other

Identifiers

NCT06843707
LungMet
2025-01-12 (Other Identifier)

Details and patient eligibility

About

This study will utilize tissue and peripheral blood samples for metabolomics analysis and establish a longitudinal metabolomics cohort at multiple critical treatment time points to comprehensively investigate the role of metabolomics in the diagnosis, prognosis, and therapeutic monitoring of lung cancer. By profiling metabolic alterations, this study aims to identify potential biomarkers for distinguishing benign and malignant lung nodules, predicting therapeutic efficacy, and assessing long-term prognosis. Key time points include initial screening for lung nodules, postoperative evaluation to predict treatment outcomes, and therapeutic monitoring to assess efficacy after medication or other interventions. Through these analyses, the study seeks to uncover underlying metabolic mechanisms and provide valuable insights into personalized lung cancer management.

Enrollment

2,500 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Signing of the informed consent form;
  2. Male or female, aged 18-75 years;
  3. Patients with lung nodules confirmed by CT examination;
  4. Good preoperative pulmonary function cooperation and complete reporting;
  5. Preoperative chest single/dual phase CT scans without significant artefacts and with complete imaging;
  6. The interval between preoperative pulmonary function and single/dual phase CT scans does not exceed one month.

Exclusion criteria

  1. Poor preoperative pulmonary function cooperation or missing reports;
  2. Preoperative chest single/dual phase CT scans exhibit significant artefacts or image omission;
  3. The interval between preoperative pulmonary function and single/dual phase CT scans exceeds one month;
  4. Complication with severe respiratory disorders (such as lung transplantation, pneumothorax, giant bullae, etc.);
  5. Coexisting with other severe functional impairments;
  6. Patients with obstructive lesions such as airway or esophageal stenosis;

(8) Medication use before pulmonary function testing that does not meet the cessation guidelines; (9) Pulmonary function report quality graded D-F.

Trial contacts and locations

1

Loading...

Central trial contact

Jianxing He, Professer

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems