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Clinical Trial Summary

This is a pilot prospective biomedical study of interventional type which includes 17 patients on 24 months (12 months of inclusion and 12 months of follow-up).

The objective of this study is to verify that the focal therapy technique used (with the help of Koelis® system) allows to obtain optimal dosimetric coverage of the prostate target (ie dose of 160 Gy +-5% delivered on the envelope isodose) evaluated by CT scan performed 30 days after implantation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01902680
Study type Interventional
Source Institut Claudius Regaud
Contact
Status Completed
Phase Phase 2
Start date August 23, 2013
Completion date June 6, 2017

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