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Recruiting

NCT Number: NCT06522334

Interstitial Lung Disease Registry Study: Prospective and Retrospective Observational Study in Austria

The goal of this registry is to systematically record epidemiological and clinical data throughout the whole interstitial lung disease course - starting with the diagnosis, therapy, follow up of lung function, symptom control, adverse events, medication, survival and death.

There are no additional interventions regarding this registry.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Klinik Floridsdorf, Vienna, Austria

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • diagnosis of interstitial lung disease
  • written informed consent

Exclusion criteria

  • to not comprehend and rightfully judge participation

Treatment and study plan

Primary outcomes

  1. Mortality

    Time frame: 10 years

    Mortality caused by interstitial lung disease

  2. Loss of lung function

    Time frame: 2 years

    FVC and DLCO loss within 24 months

Secondary outcomes

  1. Prevalence

    Time frame: 10 years

    Prevalence of the different interstitial lung diseases in Austria

  2. Response to drugs

    Time frame: 10 years

    Response to immunosuppressive/immunomodulating/antifibrotic drugs

Sponsors and collaborators

Lead sponsor

Ludwig Boltzmann Institute for Lung Health

Other

Registry information

Important dates

Study start
2024
Primary completion
2034
Study completion
2034
First posted
Jul 26, 2024
Registry last updated
Mar 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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