About this trial
Single-center, cross-sectional observational study assessing the feasibility of advanced accelerated MRI sequences versus standard ones in terms of image quality, diagnostic reliability, and acquisition time.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Consecutive adults (≥18 y.o.) admitted to the UO for W MRI for screening procedure.
Consecutive adult male patients (≥18 y.o.) admitted to the UO for WB-MRI for screening procedure and focus on prostate.
Disqualifiers
refused to consent
claustrophobia
metal prosthesis potentially affecting image quality
Trial population
Consecutive adults (≥18 years) admitted to the Advanced Imaging for Personalized Medicine Unit for screening WB-MRI, including a male subgroup undergoing prostate-focused imaging to rule out malignancy. Subjects refusing consent, with claustrophobia, or with metallic implants compromising image quality are excluded.
Trial design
Cohort
Cross-sectional
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Image quality
Comparison between standard and accelerated MRI sequences in terms of diagnostic accuracy, acquisition time.
Secondary outcomes
Image quality - subjective
Likert-scale evaluation of images between independent readers with different levvels of experience
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
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