Clinical Trial

Stereotactic Body Radiation Therapy (SBRT) for Prostate Cancer

Active, Not Recruiting
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Summary
The purpose of this study is to learn the long term efficacy and side effects associated with utilizing Stereotactic Body Radiation Therapy (SBRT) radiation for prostate cancer utilizing the Elekta Versa or Agility System. SBRT uses advanced imaging techniques to deliver targeted radiation to a tumor. The Elekta Versa and Agility Systems are approved by the Food and Drug Association (FDA) for SBRT treatment of cancer. Traditional External beam radiation therapy (EBRT) for prostate carcinoma is typically done over the course of approximately 42-45 daily treatments SBRT is a way to condense this treatment into a course of 5 treatments, delivering more dose per day.
Protocol Amendment History 7 amendments
This ClinicalTrials.gov record has been amended 7 times since 2019-03-21; most recent amendment 2025-09-08.
Status change: Recruiting → Active, Not Recruiting 2021-08-24
Trial Details
NCT Number NCT03889119
Lead Sponsor Hoag Memorial Hospital Presbyterian
Conditions Prostate Cancer
Enrollment 100 participants
Start Date 2016-10-21
Primary Completion 2023-12-31 (estimated)
Study Completion 2025-12-31 (estimated)
Updated on ClinicalTrials.gov 2025-09-15