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Clinical Trial Summary

The primary objective of this study is to evaluate the performance of HR-TRUS in detection of prostate cancer lesions relative to whole mount section after radical prostatectomy as the reference.


Clinical Trial Description

The primary objective of this study is to evaluate the performance of HR-TRUS in detection of prostate cancer lesions relative to whole mount section after radical prostatectomy as the reference. The analysis will include the detection of all prostate cancer lesions as well as the detection of significant prostate cancer lesions. With this approach it is possible to calculate the sensitivity, specificity, negative predictive value, positive predictive value and overall accuracy of the correct detection of prostate cancer in the prostate. These results are of importance when the ExactVu ultrasound scanner is to be used later for prostate cancer diagnosis using targeted biopsies. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03679819
Study type Observational
Source Institut Paoli-Calmettes
Contact Dominique Genre, MD
Phone (00) 4 91 22 37 78
Email [email protected]
Status Recruiting
Phase
Start date September 5, 2019
Completion date December 31, 2021

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