Creation of a Biospecimen Repository From Patients With Interstitial Lung Diseases (ILD)
- Conditions
- Interstitial Lung Disease
- Interventions
- Other: ILDOther: HealthyOther: Pneumonia
- Registration Number
- NCT03478826
- Lead Sponsor
- Mayo Clinic
- Brief Summary
To develop a repository of blood samples from patients with ILD to support future studies into the development of such biomarkers. Patients with pneumonia and healthy patients will also be recruited as a control group.
- Detailed Description
The proposed biospecimen repository would be derived from patients diagnosed with ILD. This is to include 500 patients in the repository, with each patient contributing one blood sample. Patients with pneumonia and healthy patients will also be recruited as a control group.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 635
- Patients with a diagnosis of ILD or any fibrotic disease of the lung or a diagnosis of pneumonia
- Patients willing to provide written informed consent
- Unwillingness/unable to give blood samples
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description ILD ILD 250 patients (male and females \>18 years of age) with the diagnosis of fibrotic DILD (IPF (n=100), fibrotic NSIP (n=50), chronic hypersensitivity pneumonia (n=20), sarcoidosis(n=50), progressive rheumatoid lung disease (n=10) and scleroderma lung disease (n=20), 10 patients with other fibrosing disease (fibrosing mediastinitis), and 50 patients with lymphangioleiomyomatosis. Healthy Healthy 100 healthy participants as a control group. Pneumonia Pneumonia 25 patients with pneumonia as a control group.
- Primary Outcome Measures
Name Time Method Future Disease Management 1 visit Reliable biomarkers to help guide treatment in ILD would be a major step forward in the management of this disease.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Mayo Clinic
🇺🇸Rochester, Minnesota, United States