Actively Recruiting

Age: 18Years +
All Genders
ID04707781

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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)
Not Eligible

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

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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)

Diagnostic Evaluation

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

Long-term Monitoring

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

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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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