Actively Recruiting

All Genders
ID06655090

Fibrotic Interstitial Lung Disease Early Recognition and Strategic Therapy Study in China

Led by Dai Huaping · Updated on 2024-10-23

10000

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

Sponsors

D

Dai Huaping

Lead Sponsor

T

The First Affiliated Hospital of Guangzhou Medical University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are conducting a large observational study focused on fibrotic Interstitial Lung Disease (f-ILD), including pneumoconiosis, to better understand the clinical characteristics linked to the development, progression, and outcomes of pulmonary fibrosis. The study aims to enroll at least 10,000 cases with continuous and regular follow-up to reveal important clinical phenotypes. It also seeks to evaluate different lung biopsy techniques and optimize histological diagnosis methods for f-ILD. This study plans to develop an artificial intelligence (AI) system for quantifying pulmonary fibrosis severity and create application software for clinical use. It will also explore and validate key molecular targets and biomarkers related to fibrosis formation. By integrating clinical features, imaging, pathology, and biomarkers, the study intends to build early recognition and progression models, intervention strategies, and guidelines applicable across the country. Participants will be followed for up to six years, during which researchers will assess outcomes such as clinical diagnostic protocols for lung tissue biopsy, prediction models, AI-based fibrosis severity evaluation using high-resolution CT scans, cohort development, and identification of important molecular targets through multi-omics analysis. The study involves regular data collection and follow-up visits to monitor disease progression and evaluate these outcomes.

CONDITIONS

Brief Title

Fibrotic Interstitial Lung Disease Early Recognition and Strategic Therapy Study in China

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed as ILD
Not Eligible

You will not qualify if you...

  • Lack of chest CT
  • Patients refused to participant

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 3 years

Participants undergo diagnostic procedures to assess fibrotic interstitial lung disease severity and characteristics.

Multiple visits over 3 years

Long-term Monitoring

Duration - Up to 6 years

Participants are monitored to observe disease progression and outcomes over time.

Periodic visits during the 6-year follow-up

Trial Site Locations

Total: 1 location

1

China-Japan Friendship Hospital

Beijing, Beijing Municipality, China, 100029

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Research Team

H

Huaping Dai, M.D. Ph.D.

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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Published Research Related To This Trial

Fibrotic Interstitial Lung Disease Early Recognition and Strategic Therapy Study in China (FIRST): protocol for a prospective, multicentre registry study.

Shiyao Wang, Xinran Zhang, Bingbing Xie...

https://pubmed.ncbi.nlm.nih.gov/41198211