About this trial
The CARE® Phantom system is a medical device system that is being developed has been designed to enable the quantitative measurement of the apparent diffusion coefficient (ADC) in the prostate of patients undergoing a multi-parametric MRI (mpMRI) scan to detect prostate cancer. The final device system will comprise three elements: a calibration mat containing phantoms and embedded monitoring software, a docking station to transfer data from the phantoms, and software as a medical device (SaMD) for calibrating the resulting mpMRI images.
In this clinical trial, patients will undergo MRI scanning in different scanners using the GSP Phantoms to provide mpMRI images and phantom data for subsequent in silico analysis. The captured images and data will be used to further develop and calibrate the GSP prototype SaMD part of the medical device system, and to establish the degree of optimised reproducibility that can be achieved.
Eligibility criteria
Qualifiers
Men aged 18 years and older undergoing investigations for PCa.
Standard of Care MRI conducted.
One or more lesions with a Likert score of 3 or above identified on clinical reports.
Planned targeted biopsy within 6 months from the date of clinical care MRI.
Disqualifiers
Prostate specific antigen (PSA) level > 20ng/ml within 6 months
Previous diagnosis of prostate cancer
Ongoing hormone treatment within 3 months prior to MRI, excluding antiandrogens or 5-alpha reductase inhibitors
Contraindication to MRI scan
Trial design
Treatments tested in this trial
- MRI
Treatment groups
Sponsors and collaborators
Gold Standard Phantoms
Lead sponsor
Bioxydyn Ltd, Manchester
Collaborator
National Cancer Imaging Translational Accelerator
Collaborator
University College London Hospitals
Collaborator
National Hospital of Neurology and Neurosurgery, Queens Square, London, UK
Collaborator