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Pulmonary Fibrosis Foundation Community Registry

NCT05382572 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 10000

Last updated 2025-04-11

No results posted yet for this study

Summary

Pulmonary fibrosis (PF) results from a diverse group of health conditions and affects the lives of patients (including those who are post lung transplant), caregivers and family members. The Pulmonary Fibrosis Foundation Community Registry will offer an online portal where participants can self-enroll and directly contribute information about their experience with PF to be compiled into a longitudinal data set for use by researchers.

Conditions

Sponsors & Collaborators

Principal Investigators

  • Kevin R Flaherty, MD · Pulmonary Fibrosis Foundation

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-07-11
Primary Completion
2027-07-01
Completion
2027-07-01

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

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 NCT05382572 on ClinicalTrials.gov