Expired Study
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Baltimore, Maryland 21287


Purpose:

This pilot study aims to investigate the diagnostic utility of 18F-DCFPyL, a novel low-molecular weight PSMA PET/CT imaging agent, in men with an elevated PSA following radical prostatectomy.


Study summary:

18F-DCFPyL is a novel low-molecular weight PSMA imaging agent. A recent study of patients with metastatic prostate cancer found that PSMA PET/CT identified more sites of disease than conventional imaging with CT, MRI and bone scan. In this study we aim to investigate 18F-DCFPyL PET/CT in patients with an elevated PSA following radical prostatectomy. During the course of this study, patients will undergo two 18F-DCPyL PET/CT scans. The first scan will take place within 45 days of staging imaging and the second will take place following six months of standard of care therapy.


Criteria:

Inclusion Criteria: - Age ≥18 years - History of adenocarcinoma of the prostate treated with radical prostatectomy - Serum PSA level ≥0.2 ng/mL at least 45 days prior to study enrollment - Completed staging evaluation with bone scan as well as CT or MRI of the abdomen and pelvis at least 45 days prior to study enrollment Exclusion Criteria: - Intention to enroll in a blinded therapeutic clinical trial - History of other malignancy diagnosed within the last three years (the exception of squamous cell or basal cell carcinoma of the skin)


NCT ID:

NCT02523924


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Baltimore, Maryland 21287
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 22, 2017

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