Tampa, Florida 33612


Purpose:

The main purpose of this study is to evaluate the safety and efficacy of focal (targeted) Radio-Frequency Ablation (RFA) in men with low or intermediate-risk, clinically localized prostate cancer.


Criteria:

Inclusion Criteria: - Men 18 years of age or older - Diagnosis of adenocarcinoma of the prostate, confirmed by H.L. Moffitt Cancer Center review - No prior treatment for prostate cancer - Eastern Cooperative Oncology Group (ECOG) performance status of 0 or1 - Prostate Cancer Clinical Stage T2a and below - PSA <10 ng/ml (this will be the prostatic specific antigen (PSA) level prompting the initial prostate biopsy) - Prostate size <60 cc on transrectal ultrasound - Pre-enrollment biopsy parameters (as per H.L. Moffitt C.C. review): Minimum of 10 biopsy cores; Gleason score 6 aor 7; Unilateral cancer (only right-sided or left-sided, not bilateral). Exclusion Criteria: - Men less than 18 years of age - Medically unfit for anesthesia - Histology other than adenocarcinoma - Biopsy does not meet inclusion criteria - Men who have received any hormonal manipulation (antiandrogens; Luteinizing Hormone Releasing Hormone (LHRH) agonist; 5-alpha-reductase inhibitors) within the previous 6 months


NCT ID:

NCT02328807


Primary Contact:

Principal Investigator
Julio Pow-Sang, M.D.
H. Lee Moffitt Cancer Center and Research Institute


Backup Contact:

N/A


Location Contact:

Tampa, Florida 33612
United States

Jesse Mocha, B.S.
Phone: 813-745-2629
Email: jesse.mocha@moffitt.org

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: November 19, 2017

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