Actively Recruiting
Ultralow Dose PET Imaging for PSMA Expression
Led by Akiva Mintz · Updated on 2025-06-04
200
Participants Needed
1
Research Sites
267 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to evaluate an investigational ultralow dose PET imaging technique for prostate cancer detection and monitoring. The main question it aims to answer is: Can the investigators optimize the timing, scan duration, and image reconstruction to reduce the radiation dose 10-100 fold of the current clinical standard? Participants will be injected with a radioactive tracer called 18F-DCFPyL and be imaged on a new type of high sensitivity PET scanner for up to 3 hours
CONDITIONS
Official Title
Ultralow Dose PET Imaging for PSMA Expression
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Ability to provide informed consent and follow study procedures
- Female participants must not be pregnant or breastfeeding
- Female participants of childbearing potential must have a negative pregnancy test
You will not qualify if you...
- Exceeded the annual radiation exposure limit of 50 mSv from prior research scans including this study
- More than four prior enrollments in this study
- Severe claustrophobia, chronic pain, or musculoskeletal conditions preventing completion of the PET scan
- Receiving concurrent PSMA-targeted therapy such as lutetium-177
- Pregnant or breastfeeding individuals
- Unable to provide informed consent
- Any condition that may affect participant safety or study integrity as judged by the investigator
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Nuclear Imaging Institute
Englewood, New Jersey, United States, 07631
Actively Recruiting
Research Team
B
Barbara Blanchfield
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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