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RECRUITING

PRospective phenotypIng and Multi-omic Endotyping of Progressive Pulmonary Fibrosis

NCT06855329 · View on ClinicalTrials.gov ↗

Study 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.

Study Locations (13)

Massachusetts

  • University of Massachusetts Chan Medical School — Worcester

Michigan

  • University of Michigan — Ann Arbor

Texas

  • University of Texas Southwestern — Dallas

Virginia

  • University of Virginia — Charlottesville

Washington

  • University of Washington — Seattle

New South Wales

  • Royal Prince Alfred Hospital — Camperdown

Queensland

  • Prince Charles Hospital — Brisbane

Victoria

  • Austin Health — Melbourne

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2025-05-01
Est. Completion 2029-12

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06855329

The ClinicalTrials.gov registry entry for NCT06855329 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 500 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Massachusetts, Worcester, which has 200 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Interstitial Lung Disease appearing as the primary indexed condition, and to 0 interventions. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06855329 reports 13 study locations spanning 13 distinct geographic areas — top geographies include Massachusetts, Michigan, Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06855329 about?

NCT06855329 is a clinical study titled "PRospective phenotypIng and Multi-omic Endotyping of Progressive Pulmonary Fibrosis". 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...

What is the current status of trial NCT06855329?

This trial is currently recruiting. The enrollment target is 500 participants. The study started on 2025-05-01. Estimated completion is 2029-12.

What conditions does trial NCT06855329 study?

This clinical trial studies the following conditions: Interstitial Lung Disease, Progressive Pulmonary Fibrosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

Who is sponsoring clinical trial NCT06855329?

This trial is sponsored by University of Massachusetts, Worcester, which has 200 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06855329 being conducted?

This trial has 13 study locations across Massachusetts, Michigan, Texas, Virginia, Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial