NCT06431555
Recruiting
Not Applicable
Magnetic Resonance Lung Function Imaging Study of Pulmonary Fibrosis Combined With Emphysema Syndrome
Beijing Chao Yang Hospital1 site in 1 country55 target enrollmentJanuary 10, 2024
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Using Functional Lung MRI to Explore Pulmonary Perfusion Changes in Patients With Pulmonary Fibrosis and Emphysema Syndrome
- Sponsor
- Beijing Chao Yang Hospital
- Enrollment
- 55
- Locations
- 1
- Primary Endpoint
- perfusion defect percentage
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
This study intends to use magnetic resonance pulmonary function imaging technology to explore imaging markers for early diagnosis of patients with CPFE. Through baseline, 6-month and 12-month follow-up examinations, the changes in magnetic resonance pulmonary function in patients with CPFE and their correlation with disease progression were explored.
Investigators
Eligibility Criteria
Inclusion Criteria
- •(1) Chest HRCT shows emphysema mainly distributed in the upper lung field, manifesting as wallless or thin-walled (wall thickness \<1 mm) low-transmittance areas with clear boundaries with normal tissue, or multiple bullae (diameter \> 1 cm), and the emphysema area/total lung volume is ≥10%; (2) interstitial pulmonary fibrosis mainly distributed in the lower lung field and subpleura, manifesting as honeycomb shadow or grid shadow, and the lung structure is destroyed , may be accompanied by traction bronchiectasis, ground glass opacities and consolidation opacities.
Exclusion Criteria
- •(1) Refusal to sign the informed consent form; (2) MRI contraindications (implanted pacemaker/defibrillator, claustrophobia, or any clinical condition that prohibits longer MRI examinations).
Outcomes
Primary Outcomes
perfusion defect percentage
Time Frame: 12 months
Calculate MRI lung perfusion defect as a percentage of the whole lung
Study Sites (1)
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