- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07762573
Dynamic Functional Imaging Phenotyping and Disease Progression Risk Assessment in COPD Using Dynamic Chest Radiography: A Multicenter Retrospective Study
August 9, 2026 updated by: Nanfang Hospital, Southern Medical University
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
Conditions
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
- Name: Laiyu Liu, Professor
- Phone Number: +86 13632102245
- Email: liulaiyu@sina.com
Study Contact Backup
- Name: Dong Yu
- Phone Number: +86 15625868995
- Email: 15625868995@163.com
Study Locations
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-
Guangdong
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Guangzhou, Guangdong, China, 510400
- Recruiting
- Nanfang Hospital, Southern Medical University
-
Contact:
- Laiyu Liu, Professor
- Phone Number: +86 13632102245
- Email: liulaiyu@sina.com
-
-
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:
- Aged 30-85 years.
- Male or female.
- Patients who underwent pulmonary function testing and dynamic chest radiography at the hospital.
Exclusion Criteria:
- Incomplete medical records.
- 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.
Collaborators
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
Additional Relevant MeSH Terms
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.