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

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.

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Key information

Conditions

Whole Body Imaging Lung MRI Prostate Vascular

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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.

Exclusion criteria

refused to consent
claustrophobia
metal prosthesis potentially affecting image quality

Treatment and study plan

Primary outcomes

Image quality

Time frame: 30 months

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

Secondary outcomes

Image quality - subjective

Time frame: 30-36 months

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

Study contacts

Contact information is provided by the study sponsor or research team.

Antonio Esposito, Medicine and Surgery

CONTACT

[email protected]

+390226436185

Sponsors and collaborators

Lead sponsor

IRCCS San Raffaele

Other

Registry information

Acronym: AITECH-MRI

Important dates

Study start: 2026
Primary completion: 2028
Study completion: 2029
First posted: Jul 1, 2026
Registry last updated: Jul 1, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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