Taiwan Interstitial Lung Disease Multi-center Investigation and Registry

NCT06476470 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 10000

Last updated 2024-06-26

No results posted yet for this study

Summary

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

Sponsors & Collaborators

  • Tri-Service General Hospital

    collaborator OTHER
  • E-DA Hospital

    collaborator OTHER
  • Chang Gung Memorial Hospital

    collaborator OTHER
  • Taichung Veterans General Hospital

    lead OTHER

Principal Investigators

  • Pin-Kuei Fu, MD., Ph.D · Taichung Veterans General Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-03-10
Primary Completion
2033-12-31
Completion
2035-12-31

Countries

  • Taiwan

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06476470 on ClinicalTrials.gov