Dynamic Functional Imaging Phenotyping and Disease Progression Risk Assessment in COPD Using Dynamic Chest Radiography: A Multicenter Retrospective Study

To evaluate the utility of DCR-derived parameters for identifying dynamic functional imaging phenotypes, assessing disease severity, and predicting the risk of disease progression in COPD.

Study Overview

Status

Recruiting

Detailed Description

Chronic obstructive pulmonary disease (COPD) is the third leading cause of death worldwide. Approximately 100 million people in China have COPD, yet the early diagnosis rate remains below 13%. This multicenter retrospective study will collect previously acquired dynamic chest radiography (DCR) images, pulmonary function test results, chest computed tomography images, symptom scores, clinical data, and follow-up outcomes from participating centers. A standardized multicenter retrospective DCR-COPD database will be established to systematically evaluate the utility of DCR-derived parameters for characterizing dynamic functional imaging phenotypes, assessing disease severity, and predicting the risk of COPD progression. The study will also provide a foundation for model development and subsequent prospective multicenter validation.

Study Type

Observational

Enrollment (Estimated)

2500

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Guangdong
      • Guangzhou, Guangdong, China, 510400
        • Recruiting
        • Nanfang Hospital, Southern Medical University
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Chronic obstructive pulmonary disease (COPD) is a heterogeneous lung condition characterized by chronic respiratory symptoms, including dyspnea, cough, and sputum production. These symptoms result from airway abnormalities, such as bronchitis or bronchiolitis, and/or alveolar abnormalities, such as emphysema, that cause persistent and often progressive airflow obstruction.

Description

Inclusion Criteria:

  1. Aged 30-85 years.
  2. Male or female.
  3. Patients who underwent pulmonary function testing and dynamic chest radiography at the hospital.

Exclusion Criteria:

  1. Incomplete medical records.
  2. Considered unsuitable for inclusion in the study at the investigator's discretion.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
COPD group
any patient who complains of dyspnea, chronic cough or sputum, a history of recurrent lower respiratory infection and/or a history of exposure to disease risk factors, Pulmonary function examination indicated that FEV1/FVC <0.7 after bronchodilator was used to confirm COPD.
PRISM group
After bronchial dilation, FEV1/FVC was ≥0.70, and FEV1%PRED was <80%.
Smoking exposure groups
Smoking history of 10 years, or without COPD, pulmonary function of COPD diagnosis standard.
Normal control group
Never-smokers without airflow limitation and with normal pulmonary function.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Exacerbation/respiratory history and event
Time Frame: At Baseline
Measurement of disease control and burden
At Baseline
FEV1 %
Time Frame: At Baseline
Measurement of lung function
At Baseline
FEV1 /FVC
Time Frame: At Baseline
Measurement of lung function
At Baseline
Emphysema
Time Frame: At Baseline
Measurement of chest CT
At Baseline
diaphragm movement
Time Frame: At Baseline
Measurement of Dynamic chest radiograph
At Baseline
lung field area
Time Frame: At Baseline
Measurement of Dynamic chest radiograph
At Baseline
lung field area change rate
Time Frame: At Baseline
Measurement of Dynamic chest radiograph
At Baseline
CAT
Time Frame: At Baseline
Measurement of questionnaires
At Baseline
SGRQ
Time Frame: At Baseline
Measurement of questionnaires
At Baseline
mMRC
Time Frame: At Baseline
Measurement of questionnaires
At Baseline
Smoking history and status
Time Frame: At Baseline
Risk factors of COPD development or lung function decline
At Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Laiyu Liu, professor, Nanfang Hospital, Southern Medical University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 3, 2026

Primary Completion (Estimated)

December 30, 2029

Study Completion (Estimated)

January 30, 2030

Study Registration Dates

First Submitted

August 9, 2026

First Submitted That Met QC Criteria

August 9, 2026

First Posted (Actual)

August 13, 2026

Study Record Updates

Last Update Posted (Actual)

August 13, 2026

Last Update Submitted That Met QC Criteria

August 9, 2026

Last Verified

August 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • NFEC-2026-570
  • 2025CR003 (Other Grant/Funding Number: Clinical Research Program of Nanfang Hospital, Southern Medical University)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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