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NCT03666234: PORTRAY

Idiopathic Pulmonary Fibrosis Registry China Study

Status unknown Last updated 11 September 2018
What this trial tests

trial in Idiopathic Pulmonary Fibrosis in 800 participants. Status unknown.

Timeline
1 July 2018
Primary endpoint
30 June 2023
30 June 2023

Quick facts

Lead sponsorDai Huaping
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment800
Start date1 July 2018
Primary completion30 June 2023
Estimated completion30 June 2023
Sites1 location across China

Conditions studied

Sponsor

Dai Huaping

Who can join

40 and older, any sex, with Idiopathic Pulmonary Fibrosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

By mean of registry of newly diagnosed Chinese IPF patients from more than 15 sites, this study aims to build IPF prospective cohort, set up normative clinical database and a biological specimen bank, and examine the clinical characteristics of newly diagnosed Chinese IPF patients, as well as the nature history, prognosis, comorbidities and complications of IPF patients in China, the current treatment pattern, burden of illness, and quality of life of Chinese IPF patients.

Publications & conference data

7 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Patient Registries in Idiopathic Pulmonary Fibrosis.
    Culver DA, Behr J, Belperio JA, Corte TJ, et al · · 2019 · cited 39× · PMID 31034241 · DOI 10.1164/rccm.201902-0431ci
  2. Idiopathic Pulmonary Fibrosis Registry China study (PORTRAY): protocol for a prospective, multicentre registry study.
    Xie B, Ren Y, Geng J, He X, et al · · 2020 · cited 15× · PMID 33177132 · DOI 10.1136/bmjopen-2020-036809
  3. Evaluation of respiratory muscle dysfunction in patients with idiopathic pulmonary fibrosis: a prospective observational study with magnetic resonance imaging.
    Yang X, Wang H, Liu A, Ni Y, et al · · 2025 · cited 1× · PMID 40087606 · DOI 10.1186/s12890-025-03572-6
  4. Basal Cells Contribute to Pulmonary Fibrosis via SP1‐Mediated Senescence‐Associated Secretory Phenotype
    Wang X, Li Y, Zhao L, Zhang X, et al · · 2026
  5. Quantitative label-free multiphoton imaging of collagen features predicts disease severity and progression in idiopathic pulmonary fibrosis.
    Liu W, Sun Y, Zhao L, Wang S, et al · · 2026 · PMID 42135759 · DOI 10.1186/s12931-026-03714-2
  6. Small airway lesions appear with the course of IPF and relate to the severity of pulmonary fibrosis progression.
    Wang X, Zhao L, Song D, Zhang X, et al · · 2025 · PMID 41073982 · DOI 10.1186/s12890-025-03939-9
  7. Small airway lesions appear with the course of IPF and relate to the severity of pulmonary fibrosis progression
    wang x, Zhao L, Song D, Zhang X, et al · · 2025 · DOI 10.21203/rs.3.rs-6653847/v1

Verify or expand the search:

Other recruiting trials for Idiopathic Pulmonary Fibrosis

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03666234.

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