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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05445817
Other study ID # ILDC-001
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 2022
Est. completion date March 2024

Study information

Verified date July 2022
Source Pulmonary Care and Research Collaborative Limited
Contact Aliaa Barakat, PhD
Phone 617-895-6636
Email aliaa.barakat@ildcollaborative.org
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The purpose of this research study is to build and maintain a registry of people with interstitial lung disease (ILD). Medical information collected for this registry may be used to advance ILD and pulmonary research and improve patient care. This is an observational registry. Participants will not receive any investigational treatments or investigational drugs as part of their participation in this registry.


Description:

The registry will contain longitudinal medical histories of ILD patients. The creation and curation of the registry with utilize release of information services, biomedical informatics methods and human expert reviews. Among the registry's long-term goals is to utilize its data and informatics resources to study and advance ILD diagnosis and treatment. The registry will be developed with a set of capabilities to consistently, repeatedly, and economically build research-grade datasets that allow cohort development from natively unstructured and non-standard phenotypic clinical and imaging data.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date March 2024
Est. primary completion date December 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - People with a confirmed diagnosis of interstitial lung disease by a primary care physician and/or pulmonologist. Exclusion Criteria: -

Study Design


Locations

Country Name City State
United States Pulmonary Care and Research Collaborative, Ltd. Boston Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
Pulmonary Care and Research Collaborative Limited Genentech, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Development and implementation of a database populated with de-identified longitudinal medical histories of interstitial lung disease patients. Up to 18 months
Secondary Advancing the understanding of the natural course and the treatments of interstitial lung diseases. Up to 18 months
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