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Observational Study of New MRI Image Processing for Pelvic Abnormalities

This observational study is looking at new image processing techniques, Adaptive Image Reconstruction (AIR Recon) Deep Learning (DL) and Sonic DL, to see if they can improve the quality of MRI scans and make them faster. These techniques are not yet approved by the FDA. The study aims to compare these new methods to current scanning techniques. You might be able to join if you are over 18 and are having an MRI for prostate screening (with no prior treatment or biopsy) or for possible endometriosis (before surgery). The study will consider itself successful if these new techniques show improved image quality and shorter scan times. The current recruitment status is unclear.

Study design
This is an observational study with a planned enrollment of 60 participants. It is not specified if it is randomized or blinded.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
The primary endpoints (image quality and scan time) are measured at Baseline, suggesting no long-term follow-up after the initial scan.

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NCT07407959

Screening and Staging of Benign vs Malignant Pelvic Abnormalities

Recruiting
Not specifiedAges 18+Observational
Mayo Clinic
~60 participants
Updated 2026-02-17 on ClinicalTrials.gov
What's tested:Non-Interventional Study

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Change in image quality (healthy volunteers)
Measured over Baseline
+1 more outcome measured

Conditions

Endometrial Carcinoma
Prostate Carcinoma

Explore related trials

Endometrial CarcinomaEndometriosisProstate Carcinoma

Where it's being run

1 sites across 1 states
Minnesota1

Study leadership

  • Candice A. Bookwalter, MD, PhD · PRINCIPAL_INVESTIGATOR · Mayo Clinic in Rochester

Who to contact

Clinical Trials Referral Office
[email protected]
855-776-0015
Email the study team

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

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)

Exclusion

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

What this trial measures

  • Change in image quality (healthy volunteers)Baseline

    Three expert radiologists will read scans (blinded to technique) and provide qualitative feedback to score image quality for standard of care (SOC) imaging, SOC with AirRecon DL, SOC with Sonic DL, and SOC with AirRecon DL and Sonic DL. Reader scoring will use a 1-5 Likert scale (1-5; 1:poor, 5:excellent).

  • Change in scan timeBaseline

    Will be considered improved if the duration of the added imaging does not exceed 10 minutes