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Clinical Trial Summary

Assessment of efficacy and safety of implantable spacers when used to reduce the radiation dose delivered to the organs at risk in prostate cancer patients undergoing radiotherapy.


Clinical Trial Description

Multi-center, retrospective, observational study for assessment of rectal dose reduction following implantation of the BioProtect Balloon Implant System ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05354427
Study type Observational
Source BioProtect
Contact
Status Completed
Phase
Start date June 18, 2020
Completion date January 1, 2022

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