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Spots Global Cancer Trial Database for CyberKnife Radiosurgery for Organ-Confined Prostate Cancer: Homogenous Dose Distribution

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Trial Identification

Brief Title: CyberKnife Radiosurgery for Organ-Confined Prostate Cancer: Homogenous Dose Distribution

Official Title: Prospective Evaluation of CyberKnife Stereotactic Radiosurgery for Low and Intermediate Risk Prostate Cancer: Homogenous Dose Distribution

Study ID: NCT00643994

Study Description

Brief Summary: The purpose of this study is to determine the effects of CyberKnife radiosurgery in patients with early stage organ-confined prostate cancer.

Detailed Description: The CyberKnife Robotic Radiosurgery System is a unique radiosurgical system capable of treating tumors anywhere in the body noninvasively and with sub-millimeter accuracy. The CyberKnife System delivers radiation using a precise targeting methodology allowing a focal treatment margin around the target, thus limiting the volume of adjacent tissue receiving high doses radiation. This in turn allows the delivery of high doses of radiation to the prostate over a short series of treatments.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

St. Joseph's Hospital and Medical Center, Phoenix, Arizona, United States

Scripps Cancer Center - CyberKnife of Southern California at Vista, La Jolla, California, United States

The CyberKnife at Newport Diagnostic Center, Newport Beach, California, United States

Georgetown University, Washington, District of Columbia, United States

Coastal CyberKnife and Radiation Oncology, Fort Pierce, Florida, United States

Jupiter Medical Center & CyberKnife Center of Palm Beach, Jupiter, Florida, United States

Northwest Community Hospital, Arlington Heights, Illinois, United States

Community Cancer Center, Normal, Illinois, United States

Central Baptist Hospital, Lexington, Kentucky, United States

Sinai Hospital of Baltimore, Baltimore, Maryland, United States

Franklin Square Hospital Center, Baltimore, Maryland, United States

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States

St. Joseph Mercy Hospital, Ann Arbor, Michigan, United States

Lake Saint Louis Oncology, Saint Louis, Missouri, United States

Saint Louis University, Saint Louis, Missouri, United States

St. Mary's Regional Medical Center, Reno, Nevada, United States

Capital Health, Trenton, New Jersey, United States

Hematology Oncology Associates of Central New York, Syracuse, New York, United States

Virginia Hospital Center, Arlington, Virginia, United States

Swedish Cancer Center, Seattle, Washington, United States

Southwest Washington Medical Center, Vancouver, Washington, United States

Southwest Washington Regional Cancer Center, Vancouver, Washington, United States

ThedaCare Appleton Medical Center, Appleton, Wisconsin, United States

Contact Details

Name: Robert Meier, MD

Affiliation: Swedish Cancer Center

Role: STUDY_CHAIR

Name: Irving Kaplan, MD

Affiliation: Beth Israel Deaconess Medical Center

Role: STUDY_CHAIR

Name: Martin Sanda, MD

Affiliation: Beth Israel Deaconess Medical Center

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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