The Clinical Value of Deep Learning-Based Reconstruction Techniques in Cardiac MRI Scanning
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Cardiac Disease. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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
Primary outcome measures
- Patient satisfaction [Time frame: immediately after procedure]
Secondary outcome measures (2)
- total scan time [Time frame: During procedure]
- objective image measurements (signal-to-noise ratio) [Time frame: one week]
Eligibility criteria
Inclusion criteria
- Patients requiring cardiac MRI in clinical practice;
- Patient age ≥ 18 years;
- The patient has signed an informed consent form.
Exclusion criteria
- 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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-control
Study locations
China · 1 center
- Union Hospital，Tongji Medical College，Huazhong University of Science and Technology — Wuhan
Identifiers
NCT: NCT07274436 · 2025-0804