AI Technologies for Enhanced and Celerated High-Field WB-MRI

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorIRCCS San Raffaele

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Image quality

Comparison between standard and accelerated MRI sequences in terms of diagnostic accuracy, acquisition time.

Time frame
30 months

Secondary outcomes

1

Image quality - subjective

Likert-scale evaluation of images between independent readers with different levvels of experience

Time frame
30-36 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

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