Actively Recruiting
Assessment the Effectiveness of BTVA in COPD and Ablation in Pulmonary Nodules by Pulmonary MRI
Led by Shanghai Chest Hospital · Updated on 2025-07-01
100
Participants Needed
1
Research Sites
108 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
A Clinical Study Based on Magnetic Resonance Imaging of the Lungs to Assess the Efficacy of Thermal Vapor Ablation and Pulmonary Nodule Ablation in Chronic Obstructive Pulmonary Disease After Surgery. The efficacy of hot steam ablation for chronic obstructive pulmonary disease was evaluated using the innovative MRI sequence PREFUL\_MRI, and the efficacy of pulmonary nodule ablation was evaluated using the innovative MRI sequence GRASP\_MRI.
CONDITIONS
Official Title
Assessment the Effectiveness of BTVA in COPD and Ablation in Pulmonary Nodules by Pulmonary MRI
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years old
- Patients with pulmonary nodules indicated by chest CT, pathologically diagnosed as malignant, and receiving ablative treatment including radiofrequency, microwave, or freezing
- Patients diagnosed with COPD according to the GOLD principle and treated with thermal steam ablation
- Understand the study and provide informed consent
You will not qualify if you...
- Pulmonary nodules that are pure ground glass nodules on chest CT
- Presence of metal implants such as cardiac pacemakers, heart stents, artificial heart valves, or conditions like claustrophobia or allergy to contrast media making MRI unsuitable
- Severe cardiopulmonary dysfunction or other diseases that significantly increase ablation surgery risk
- Severe COPD exacerbation or pneumonia within the past four weeks
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Shanghai chest hospital
Shanghai, Shanghai Municipality, China, 200030
Actively Recruiting
Research Team
L
Lin Ye, MD
CONTACT
J
Jiayuan Sun, MD, PhD
CONTACT
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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