Actively Recruiting

Age: 18Years +
All Genders
ID00258583

Dorothy P. and Richard P Simmons Center for Interstitial Lung Disease Research Registry

Led by University of Pittsburgh · Updated on 2025-10-29

5000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to collect past, current, and future medical records from individuals treated for interstitial lung disease at the UPMC Simmons Center for Interstitial Lung Disease. The goal is to create a research registry that will help investigators better understand interstitial lung disease and its treatment by studying a large collection of patient data. This registry also supports identifying and recruiting patients for future research studies related to this lung condition. Participants provide permission for their medical records to be included in this research registry. There are no specific treatments or interventions as this is an observational study focused on gathering medical information rather than administering therapies. The registry will continuously collect data from the participants' records over time. During the study, researchers will review the medical records of participants to answer questions about interstitial lung disease. There are no required visits, procedures, or treatments since the study involves only the collection and analysis of medical data. Participation may continue over many years, with ongoing updates to the registry as new medical information becomes available.

CONDITIONS

Brief Title

Dorothy P. and Richard P. Simmons Center for ILD Research Registry

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients who are seeking treatment at the UPMC Simmons Center for Interstitial Lung Disease
  • 18 years of age or older
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Long-term Monitoring

Duration - Up to July 2035

Participants' past, current, and future medical record information is collected and observed to support research on interstitial lung disease.

Trial Site Locations

Total: 1 location

1

Michelle F MacPherson

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

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Research Team

M

Michelle F MacPherson, MAT

M

Michelle Meyers, BSN, RN

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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