Acute Interstitial Pneumonia Clinical Trials

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PRIME-PPF: PRospective phenotypIng and Multi-omic Endotyping of Progressive Pulmonary Fibrosis

Status: Recruiting
Location: See all (23) locations...
Study Type: Observational
SUMMARY

This is a prospective, observational cohort study. Participants with non-idiopatic pulmonary fibrosis, interstitial lung disease (ILD) will be followed for 24 months to systematically collect clinical, imaging, and biospecimen data. The primary objective is to optimize progressive pulmonary fibrosis (PPF) classification and establish PPF incidence for key ILD subtypes. Additional exploratory objectives are to 1) Prospectively validate a novel PPF classifier and assess performance durability over time, and 2) Determine whether multi-dimensional PPF prediction outperforms component approaches.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Age 18-80 years with a diagnosis of non-IPF fibrosing ILD due to CTD-ILD, fHP, or non-IPF IIP based on central review

• Diagnosis of Fibrotic ILD as determined by site investigator.

• Willingness to comply with study procedures and follow-up.

• Provide written informed consent.

Locations
United States
Colorado
University of Colorado | Anschutz Medical Campus
NOT_YET_RECRUITING
Aurora
Massachusetts
University of Massachusetts Chan Medical School
RECRUITING
Worcester
Michigan
University of Michigan
RECRUITING
Ann Arbor
New York
Weill Cornell Medicine
NOT_YET_RECRUITING
New York
Texas
University of Texas Southwestern
RECRUITING
Dallas
Virginia
University of Virginia
RECRUITING
Charlottesville
Washington
University of Washington
RECRUITING
Seattle
Other Locations
Australia
Prince Charles Hospital
NOT_YET_RECRUITING
Brisbane
Royal Prince Alfred Hospital
NOT_YET_RECRUITING
Camperdown
Austin Health
NOT_YET_RECRUITING
Melbourne
Austria
Medical University of Graz
NOT_YET_RECRUITING
Graz
Canada
University of British Columbia
RECRUITING
Vancouver
Denmark
Aarhus University Hospital
NOT_YET_RECRUITING
Aarhus
France
Bichat, APHP
NOT_YET_RECRUITING
Paris
Chu Pontchaillou
NOT_YET_RECRUITING
Rennes
Germany
Prüfzentrum der GWT am Lungenzentrum Coswig
NOT_YET_RECRUITING
Coswig
University Medical Center Mainz
RECRUITING
Mainz
LMU Munich
NOT_YET_RECRUITING
Munich
Hungary
Semmelweis University
NOT_YET_RECRUITING
Budapest
Ireland
University College Dublin
RECRUITING
Dublin
Italy
Rimini and Riccione Hospitals, AUSL Romagna
NOT_YET_RECRUITING
Rimini
Netherlands
Erasmus MC
RECRUITING
Rotterdam
Spain
Hospital Universitario de La Princesa
NOT_YET_RECRUITING
Madrid
Contact Information
Primary
Fernando J Martinez, MD, MS
fernando.martinez1@umassmed.edu
508-334-8685
Backup
Elizabeth Peters, BSN
elizabeth.peters2@umassmed.edu
774-455-4432
Time Frame
Start Date: 2025-05-01
Estimated Completion Date: 2029-12
Participants
Target number of participants: 500
Sponsors
Leads: University of Massachusetts, Worcester
Collaborators: Fondazione Policlinico Universitario Agostino Gemelli IRCCS, University of Michigan, Johannes Gutenberg University Mainz, University of Virginia

This content was sourced from clinicaltrials.gov