UVA Natural History Study for Interstitial Lung Diseases
This study at the University of Virginia is observing people with Interstitial Lung Disease (ILD), including Idiopathic Pulmonary Fibrosis (IPF), Sarcoidosis, Connective Tissue Diseases, and Hypersensitivity Pneumonitis. Researchers are collecting information and samples over time to better understand how these diseases progress and how different treatments might affect them. They are also including family members without ILD as a comparison group. The goal is to identify trends that could lead to a better understanding of disease progression, treatment options, and outcomes. This is an observational study, meaning there are no interventions or new treatments being tested. The study is currently enrolling up to 2500 participants.
- Study design
- This is an observational study with a planned enrollment of 2500 participants. It is not testing any specific intervention.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- You would be followed yearly from the date of consent until you are lost to follow-up or death occurs, for up to 144 months (12 years).
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
University of Virginia Natural History Study
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Imre Noth, MD · PRINCIPAL_INVESTIGATOR · University of Virginia Health System
- Yousef Althulth, MD · STUDY_DIRECTOR · University of Virginia Health System
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Clinical Course of DiseaseYearly from date of consent until subject is lost to follow-up or death occurs, whichever comes first, assessed up to 144 months
Course of disease in patients with ILD will be reviewed prospectively for the duration of the study
- Subject deathsYearly from date of consent until subject is lost to follow-up or death occurs, whichever comes first, assessed up to 144 months
Causes of death in patients with ILD will be reviewed prospectively for the duration of the study