Actively Recruiting
Taiwan Interstitial Lung Disease Multi-center Investigation and Registry
Led by Taichung Veterans General Hospital · Updated on 2024-06-26
10000
Participants Needed
1
Research Sites
616 weeks
Total Duration
On this page
Sponsors
T
Taichung Veterans General Hospital
Lead Sponsor
T
Tri-Service General Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
The Taiwan Interstitial Lung Disease (ILD) Multi-center Investigation and Registry aims to evaluate the long-term outcomes of patients with fibrotic interstitial lung disease. This prospective observational registry will collect comprehensive clinical data from multiple centers, including epidemiological information, comorbidities, questionnaire results, routine blood tests, biochemical tests, pulmonary function tests, echocardiograms, and cardiopulmonary exercise tests (CPET), all following a standardized protocol. Key components of the registry include annual HRCT scans, annual CPETs, biobank blood samples, and biannual echocardiograms and pulmonary function tests. The main questions the registry aims to answer are: 1. Differences in all-cause mortality among ILD patients of different etiologies. 2. Differences in the annual risk of acute exacerbation among ILD patients of different etiologies. 3. Effectiveness of current anti-fibrotic drugs in treating IPF and ILD of different etiologies. 4. Predictive ability of HRCT imaging features for mortality risk in ILD patients. 5. Impact of comorbidities on the mortality risk of ILD patients. 6. Predictive ability of biomarkers for disease progression and mortality.
CONDITIONS
Official Title
Taiwan Interstitial Lung Disease Multi-center Investigation and Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years old
- Diagnosed with interstitial lung disease (ILD) by a pulmonologist, rheumatologist, or radiologist
- Diagnosed with any cause of ILD including idiopathic pulmonary fibrosis (IPF), connective tissue disease-associated ILD (CTD-ILD), unclassified ILD, drug-induced ILD, lymphangioleiomyomatosis (LAM), or sarcoidosis-associated ILD
You will not qualify if you...
- Under 18 years old
- Unable to provide informed consent personally
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Taichung Veterans General Hospital
Taichung, Taiwan, 40705
Actively Recruiting
Research Team
P
Pin-Kuei Fu, MD., Ph.D
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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