Actively Recruiting

Age: 18Years +
All Genders
ID04654364

Lung Cancer Registry Observational Study to Collect Patient Treatment and Outcome Data

Led by Arbeitsgemeinschaft medikamentoese Tumortherapie · Updated on 2025-04-10

500

Participants Needed

3

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Lung cancer is a serious condition affecting many people, with high mortality rates, particularly in Austria. This observational registry study is designed to collect and analyze data from patients diagnosed with lung cancer, including non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC). The goal is to better understand patient characteristics, molecular testing, treatment patterns, and outcomes to improve personalized treatment strategies. This study collects routine medical and treatment information from patient charts without requiring additional diagnostic or therapeutic interventions. Data will be gathered from multiple centers and include longitudinal follow-up until patient death or loss to follow-up. No changes to patient treatment are made, as the study only observes and records existing care. Participants will have their medical data documented in an electronic registry with confidentiality maintained through unique patient identifiers. Researchers will assess various outcomes over 10 years, including treatment duration, frequency, response, sequence, survival (overall survival and progression-free survival), and treatment toxicity. No extra procedures are required, and participation does not interfere with standard care.

CONDITIONS

Brief Title

Lung Cancer Registry

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with stage III A-C or IV A-B non-small cell lung cancer (NSCLC)
  • Diagnosed with limited disease (LD) or extensive disease (ED) small cell lung cancer (SCLC)
  • 18 years of age or older
Not Eligible

You will not qualify if you...

  • No specific exclusion criteria due to the non-interventional design of the registry

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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)

Long-term Monitoring

Duration - Up to 10 years

Participants who undergo routine care are observed. Measurements and data are collected from existing medical records over time to track treatment and outcomes.

Data collected from routine healthcare visits and medical records

Trial Site Locations

Total: 3 locations

1

Universitätsklinik für Innere Medizin III, PMU Salzburg

Salzburg, State of Salzburg, Austria, 5020

Actively Recruiting

2

Univ.-Klinik für Innere Medizin V, Hämatologie/Onkologie LKH-Innsbruck / Universitätskliniken

Innsbruck, Tyrol, Austria, 6020

Actively Recruiting

3

Kepler Universitätsklinikum GmbH, Med. Campus III, Klinik für Lungenheilkunde / Pneumologie

Linz, Upper Austria, Austria, 4021

Actively Recruiting

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Research Team

D

Daniela Wolkersdorfer

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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