Screening and Staging of Benign vs Malignant Pelvic Abnormalities
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorMayo Clinic
About this trial
This study evaluates whether newly developed non-FDA approved image processing techniques \[Adaptive Image Reconstruction (AIR Recon) Deep Learning (DL) and Sonic DL\] can provide improved quality and decreased time compared to current scanning techniques.
Eligibility criteria
Qualifiers
Patient over the age of 18
For prostate group, any patient referred for prostate MR for screening purposes with no prior prostate related treatment or prior biopsy
For endometriosis group, any patient referred for possible endometriosis evaluation (pre-surgical)
Disqualifiers
Individuals unable to undergo MRI imaging (MR-conditional or MR-nonconditional devices which would need additional procedures/conditions for scanning, pregnant people, individuals with implanted metal, etc.)
Patient under the age of 18
Patient who is unable to consent
Trial design
Treatments tested in this trial
- Non-Interventional Study
Treatment groups
60 Participants
are divided into 1 treatment groupLocations
1Mayo Clinic in Rochester55905, RochesterMinnesota, United States
Sponsors and collaborators
Mayo Clinic
Lead sponsor
Source ClinicalTrials.gov