Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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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