Stratagen Quantitative Prostate MRI Platform Pilot Study
Conditions
Prostate CancerSummary
The goal of this clinical trial is to assess the safety and feasibility of the Stratagen Quantitative Prostate MRI Platform when used in addition to the standard scans conducted during the existing prostate MRI sessions.* What severe problems, if any, occur because of the use of the Stratagen Quantitative Prostate MRI Platform? * Can the data collected be used to measure quantitative MRI parameters?Participants will:- Receive up to 15 minutes of additional MRI scan time during the existing prostate MRI imaging session.
Locations
1 location Found with status Recruiting
Eligibility Criteria
Inclusion Criteria:
* Subject has a prostate that would be considered for biopsy
* Age 40-90 years
* PSA ≥ 2.5
* Subject has been informed of the nature of the study and has provided written informed consent
Exclusion Criteria:
* Contraindication for MRI
* Prostate biopsy within the previous 12 weeks
* Implant in the pelvis that may cause artifact on MRI (e.g. hip replacement)
* History of prostatectomy or other local prostate cancer therapy (e.g., cryotherapy or brachytherapy), or previous pelvic irradiation
* Currently enrolled in another investigational drug or device study that clinically interferes with this study
* Unable to comply with the study requirements or follow up schedule
* Any condition the Investigator believes would interfere with the intent of this study or would make participation not in the best interest of the subject
Study Plan
Stratagen Quantitative Prostate MRI Platform
DEVICE:
MRIDescription:
Will receive up to 15 minutes of additional MRI scan time during the existing prostate MRI imaging session.
Outcome Measures
Primary Outcome Measures
Safety: no SAEs attributable to the Stratagen Quantitative Prostate MRI Platform, as determined by participating Investigator according to CTCAE guidelines
u2022 Feasibility: collection of the data necessary to produce measurable quantitative T1 and T2 relaxation times (milliseconds) maps (images) for at least 80% of pixels fully contained within the prostate for at least 80% of subjects
Timeline
Last Updated
October 21, 2025Start Date
May 22, 2025Today
December 16, 2025Completion Date ( Estimated )
October 31, 2026
Sponsors of this trial
Lead Sponsor
Stratagen Bio, Inc.