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18F-rhPSMA-7.3 PET/MRI for Prostate Cancer Active Surveillance
Study Summary
This trial studies how PET/MRI with an imaging drug and MRI contrast can help diagnose prostate cancer in those eligible for active surveillance. Not a treatment trial.
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
Media Library
- I have been treated for prostate cancer.My prostate cancer requires treatment beyond just watching.I am a man with low or favorable intermediate risk prostate cancer scheduled for a detailed prostate MRI and biopsy.I am suspected to have prostate cancer but it hasn't been confirmed with a biopsy.
- Group 1: Prostate Cancer
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Are individuals under 30 years of age being included in the current research study?
"This trial has an age range of 18-89, and is thus available to adult patients."
Is it still possible to submit an application for this research study?
"According to the information provided on clinicaltrials.gov, recruiting for this medical trial has ceased. Having been first posted in March of 2023 and last updated January 21st, it is among a pool of 1,294 other trials currently searching for enrollees."
Is participation in this experiment feasible for me?
"Currently, this clinical trial is searching for 30 male individuals with prostate cancer between 18 and 89 years old. The specific inclusion criteria are as follows: Men who have had a biopsy that confirms low risk or favourable intermediate risk prostate cancer, scheduled to undergo multiparametric MRI scans followed by confirmatory biopsies in accordance with institutional active surveillance protocols."
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