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The purpose of ths study is to evaluate and compare the performance characteristics of the available FDA approved transperineal biopsy devices.
The purpose of this study is to assess safety and initial effectiveness of the DynaCAD /UroNAV ablation planning and guidance system aided cryo-ablation in the treatment of low to intermediate risk, localized (organ confined) prostate cancer tumors.
The purpose of this study is to evaluate the detection rates of MRI-targeted prostate biopsies compared to standard 12-core trans-rectal ultrasound guided (TRUS) prostate biopsies for prostate cancer.
This prospective clinical trial (PRostate Imaging using Mri +/- contrast Enhancement (PRIME)) aims to assess whether biparametric MRI (bpMRI) is non-inferior to multiparametric mpMRI (mpMRI) in the detection of clinically significant prostate cancer.
The purpose of this study is to evaluate the safety and efficacy of a single treatment of PRX302 for the treatment of Benign Prostatic Hyperplasia (BPH) as compared to placebo.
This study will attempt to identify potential non-pharmacologic interventions that will decrease the morbidity associated with prostate biopsy.