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Clinical Trial Summary

This study is being conducted to determine whether the combination of imaging agents 68-Ga RM2 and 68-Ga PMSA11 is better at assessing response to high intensity focused ultrasound (HIFU) or high dose rate (HDR) local therapy than standard imaging or biopsy in patients with known prostate cancer.


Clinical Trial Description

Primary Objective: To determine feasibility of 68Ga-PSMA-11 PET/MRI and 68Ga-RM2 PET/MRI for evaluation of HIFU or HDR local therapy in patients with known prostate cancer. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03949517
Study type Interventional
Source Stanford University
Contact Shahryar Niknam
Phone 650-721-4080
Email sniknam@stanford.edu
Status Recruiting
Phase Phase 1/Phase 2
Start date April 9, 2019
Completion date October 2022

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