Actively Recruiting

Age: 18Years - 75Years
All Genders
ID06843707

Establishing a Longitudinal Cohort Study of Lung Cancer Using Tissue and Peripheral Blood Metabolomics to Explore Biomarkers and Therapeutic Mechanisms.

Led by The First Affiliated Hospital of Guangzhou Medical University · Updated on 2025-02-25

2500

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the role of metabolomics in lung cancer by analyzing tissue and peripheral blood samples at key treatment stages. The study aims to identify metabolic changes that could serve as biomarkers to distinguish between benign and malignant lung nodules, predict treatment effectiveness, and assess long-term outcomes. This observational research is conducted by The First Affiliated Hospital of Guangzhou Medical University to enhance personalized lung cancer care. The study involves monitoring serum metabolites using tissue and blood samples collected at critical points such as initial lung nodule screening, after surgery to evaluate treatment results, and during ongoing therapy to assess its impact. These metabolic profiles are analyzed to uncover differences linked to disease progression and response to treatment, helping to understand underlying mechanisms and develop better diagnostic and prognostic tools. Participants will provide tissue and blood samples at these defined times, allowing researchers to track metabolic alterations over several years. The primary outcome measure is the area under the curve over 3 years, with secondary outcomes including identification of differentially expressed metabolites during this period. This long-term follow-up aims to provide insights into how metabolomics can improve diagnosis, prognosis, and therapy monitoring in lung cancer patients.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed informed consent form
  • Male or female aged 18 to 75 years
  • Patients with lung nodules confirmed by CT examination
  • Good cooperation with preoperative pulmonary function testing and complete reports
  • Preoperative chest single or dual phase CT scans without significant artefacts and complete imaging
  • Interval between preoperative pulmonary function and CT scans not exceeding one month
Not Eligible

You will not qualify if you...

  • Poor cooperation with preoperative pulmonary function testing or missing reports
  • Preoperative chest single or dual phase CT scans with significant artefacts or missing images
  • Interval between preoperative pulmonary function and CT scans exceeding one month
  • Severe respiratory disorders such as lung transplantation, pneumothorax, or giant bullae
  • Other severe functional impairments
  • Obstructive lesions like airway or esophageal stenosis
  • Use of medication prior to pulmonary function testing that does not meet cessation guidelines
  • Pulmonary function report quality graded D-F

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 3 years

Participants have tissue and peripheral blood samples collected to monitor serum metabolites associated with lung cancer progression and treatment response.

Periodic visits for sample collection and assessments over the study period

Trial Site Locations

Total: 1 location

1

the First Affiliated of Guangzhou Medical University

Guangzhou, Guangdong, China, 510120

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Research Team

J

Jianxing He, Professer

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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