Actively Recruiting
Clinical Database for Early Recognition of Lung Involvement in Patients at Risk for Interstitial Lung Disease
Led by Medical University of Graz · Updated on 2026-01-15
412
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
M
Medical University of Graz
Lead Sponsor
B
Boehringer Ingelheim
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are establishing a clinical database and screening program for patients at risk of Interstitial Lung Disease (ILD), particularly those with systemic diseases that may lead to lung involvement. The study aims to collect detailed clinical data to enhance early detection and understanding of ILD progression. This observational research is sponsored by the Medical University of Graz and focuses on improving patient care through early recognition of lung problems. Participants will be grouped into those undergoing a prospective ILD screening algorithm and those with a prior ILD diagnosis. The study uses chest CT scans to assess lung involvement and observe changes over time. This prospective screening approach helps identify early lung changes in at-risk patients, while the retrospective group provides additional clinical insights. During the study, participants will have lung function measured, including the carbon monoxide diffusing capacity (DLCO) and forced vital capacity (FVC) at the time of ILD diagnosis, with follow-up planned for up to 5 years. Researchers will gather clinical data, imaging results, and lung function tests to monitor disease progression and outcomes. Total participation duration varies, with ongoing data collection to support early diagnosis and better management of ILD.
CONDITIONS
Brief Title
Database for Interstitial Lung Disease
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Patients with a known systemic disease bearing a risk for Interstitial Lung Disease
- Signed informed consent (for prospective part)
You will not qualify if you...
- Age under 18 years
- Comorbidities severely limiting life expectancy, such as severe cardiovascular conditions or malignant disease
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 5 years
Participants undergo assessment of interstitial lung disease using chest CT scans.
Visits scheduled according to clinical need over the course of the study
Duration - Up to 5 years
Participants are monitored for lung function and disease progression over time.
Periodic assessments during follow-up visits
Trial Site Locations
Total: 1 location
1
Medical University of Graz, Department of Internal Medicine, Division of Pulmonology
Graz, Austria, 8036
Actively Recruiting
Research Team
G
Gabor Kovacs, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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