The Clinical Value of Deep Learning-Based Reconstruction Techniques in Cardiac MRI Scanning
1 other identifier
observational
50
1 country
1
Brief Summary
By enrolling patients who underwent cardiac MR(Magnetic Resonance) examinations at our center and using randomized allocation, the patients were divided into a study group and a control group. The study group underwent scanning using AI-based(Artificial Intelligence-based) cardiac MRI(Magnetic Resonance Imaging) sequences, while the control group was scanned using non-AI cardiac MRI sequences
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Aug 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2025
CompletedFirst Submitted
Initial submission to the registry
November 19, 2025
CompletedFirst Posted
Study publicly available on registry
December 10, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2026
December 10, 2025
November 1, 2025
1 year
November 19, 2025
November 27, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Patient satisfaction
Patient satisfaction will be evaluated using a Likert scale with the following scoring criteria:5 - Very Satisfied;4 - Satisfied;3 - Neutral;2 - Dissatisfied;1 - Very Dissatisfied
immediately after procedure
Secondary Outcomes (2)
total scan time
During procedure
objective image measurements (signal-to-noise ratio)
one week
Study Arms (2)
scanning using AI-based cardiac MRI sequences
scanning using non-AI cardiac MRI sequences
Eligibility Criteria
Patients requiring cardiac MRI in clinical practice
You may qualify if:
- Patients requiring cardiac MRI in clinical practice;
- Patient age ≥ 18 years;
- The patient has signed an informed consent form.
You may not qualify if:
- Patients with contraindications to magnetic resonance imaging;
- Patients who failed to complete the MRI examination or whose image quality was inadequate for diagnostic requirements;
- Other circumstances deemed by clinical trial personnel as unsuitable for participation in this trial;
- Subjects or their legal guardians voluntarily requesting to withdraw.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Lian Yanglead
Study Sites (1)
Union Hospital,Tongji Medical College,Huazhong University of Science and Technology
Wuhan, Hubei, 430000, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Director
Study Record Dates
First Submitted
November 19, 2025
First Posted
December 10, 2025
Study Start
August 1, 2025
Primary Completion (Estimated)
August 1, 2026
Study Completion (Estimated)
August 1, 2026
Last Updated
December 10, 2025
Record last verified: 2025-11