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Radiation Therapy
CyberKnife for Prostate Cancer
N/A
Waitlist Available
Led By Afshin Rashtian, MD
Research Sponsored by Riverside Community Hospital, California
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 5 years
Awards & highlights
Study Summary
The purpose of this study is to determine the side effects and how effective CyberKnife stereotactic ablative body radiation (SABR) is in patients with prostate cancer. The CyberKnife system is a new type of radiation machine that uses a special system to precisely focus large doses of x-rays on the tumor. The device is designed to concentrate large doses of radiation onto the tumor so that injury from radiation to the nearby normal tissue will be minimal. The purpose of this evaluation is to see if this treatment will help patients with low to intermediate risk prostate cancer and to evaluate the effect of this treatment on the patients' quality of life over time.
Eligible Conditions
- Prostate Cancer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~5 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
CyberKnife Toxicities in Prostate Cancer
Secondary outcome measures
Cancer Control and Quality of Life (Composite)
Trial Design
1Treatment groups
Experimental Treatment
Group I: CyberKnifeExperimental Treatment1 Intervention
CyberKnife Stereotactic Ablative Body Radiation Therapy
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Who is running the clinical trial?
Riverside Community Hospital, CaliforniaLead Sponsor
Afshin Rashtian, MDPrincipal InvestigatorUnaffilated
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