Your session is about to expire
← Back to Search
Device
Proxiscan device for Prostate Cancer
Phase < 1
Waitlist Available
Led By Benjamin Franc, MD
Research Sponsored by Radiological Associates of Sacramento Medical Group Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up within on month of scan and corresponding mri
Awards & highlights
No Placebo-Only Group
Summary
This is a small study to determine if probe, similar to an ultrasound probe, can detect prostate cancer more specifically than other imaging studies in patients with a positive prostate cancer biopsy.
Eligible Conditions
- Prostate Cancer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ within on month of scan and corresponding mri
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~within on month of scan and corresponding mri
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Detection of PSMA antibody (ProstaScint)uptake patterns measured by Proxiscan in comparison with anatomic biopsy reports, conventional SPECT and MRI scans within one month of Proxiscan
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Active Control
Group I: No interventionActive Control1 Intervention
All consenting patients will be imaged with the Proxiscan and data compared with MRI, ProstaScint and biopsy data
Find a Location
Who is running the clinical trial?
Hybridyne Imaging TechnologiesUNKNOWN
Radiological Associates of Sacramento Medical Group Inc.Lead Sponsor
Benjamin Franc, MDPrincipal InvestigatorRadiological Associates of Sacramento Medical Group Inc.
Share this study with friends
Copy Link
Messenger