Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Prostate Cancer
Type
Interventional
Phase
Not Applicable
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Only males

Description

Expected benefit(s) of the trial Improved quality of life during brachytherapy on account of the absence of radioactive seeds in the prostate: Fewer early urinary complications, No urine filtration, No post-operative use of condoms, No 2-year ban on cremation following treatment, Health cost savings...

Expected benefit(s) of the trial Improved quality of life during brachytherapy on account of the absence of radioactive seeds in the prostate: Fewer early urinary complications, No urine filtration, No post-operative use of condoms, No 2-year ban on cremation following treatment, Health cost savings, Acquisition of dosimetric data for inverse optimization. Predictable risk(s) for patients Predictable risks in the context of this trial involve the frequency of essentially urinary disorders. Methodology Open, monocentric, phase I-II study.

Tracking Information

NCT #
NCT02104362
Collaborators
Not Provided
Investigators
Not Provided