RSSearch Patient Registry-Long Term Study of Use of SRS/SBRT



Status:Enrolling by invitation
Conditions:Cancer, Cardiology, Hematology
Therapuetic Areas:Cardiology / Vascular Diseases, Hematology, Oncology
Healthy:No
Age Range:Any
Updated:4/21/2016
Start Date:March 2012
End Date:December 2025

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Multi-Institution Registry of SRS/SBRT Procedures

The RSSearch® Registry is an international multi-year database designed to track SRS/SBRT
(Stereotactic Radiosurgery/Stereotactic Body Radiation Therapy) utilization, treatment
practices and outcomes to help determine, over time, the most effective use of these systems
in management of patients with life threatening tumors and other diseases. (This study was
formally called ReCKord and included the CyberKnife only; The ReCKord study continues as a
CyberKnife subset of RSSearch.)

The Registry is designed to help SRS/SBRT (Stereotactic Radiosurgery/Stereotactic Body
Radiation Therapy) users to understand utilization of and key treatment outcomes for these
treatment approaches. Some of the objectives include:

Allow participants to record information about usage of SRS/SBRT in everyday practice,
including patient characteristics and disease information, treatment plans and outcomes
Provide participants with ready access to data for publication of their own experience and
as a tool for establishing collaborations with other participating sites Facilitate quality
improvement efforts for individual treatment providers Understand the effectiveness of
different treatment plans for different types of lesions, diseases and treatments

The Registry tracks select outcomes for each condition treated by SRS/SBRT (for example, PSA
for prostate cancer); the Registry also provides individual participants the ability to add
additional outcomes for each and any condition of specific interest to their institutions.

The Registry is hosted by Advertek, Inc who is an independent vendor of electronic
registries; they are responsible for HIPAA compliance, including all security mechanisms.

Patients will be enrolled prospectively. Some retrospective patient data is likely to be
included in order to capture both short and longer term outcomes data.

Inclusion Criteria:

- Diagnosis of benign or malignant tumors or other conditions deemed treatable by
stereotactic radiosurgery or stereotactic body radiotherapy

- Willingness to sign an Informed Consent Document

Exclusion Criteria:

- There are no specific exclusion criteria, but patients who are unwilling to sign the
ICD will not be included
We found this trial at
22
sites
534 Biltmore Avenue
Ashville, North Carolina 28801
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Ashville, NC
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3550 Jerome Avenue
Bronx, New York 10467
(718) 920-4321
Montefiore Medical Center As the academic medical center and University Hospital for Albert Einstein College...
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Bronx, NY
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Baltimore, Maryland 21237
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Baltimore, MD
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Brunswick, Georgia 31520
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Brunswick, GA
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Chattanooga, Tennessee 37403
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Chattanooga, TN
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Colorado Springs, Colorado 80907
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Colorado Springs, CO
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Elmhurst, Illinois 60126
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Elmhurst, IL
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Grand Rapids, Michigan 49503
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Grand Rapids, MI
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Harrisburg, Pennsylvania 17101
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Harrisburg, PA
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Hollywood, Florida 33021
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Hollywood, FL
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Huntington, West Virginia 25702
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Huntington, WV
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Lafayette, Colorado 80026
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Lafayette, CO
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Memphis, Tennessee 38119
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Memphis, TN
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Nedlands,
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Oklahoma City, Oklahoma 73102
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Oklahoma City, OK
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Philadelphia, Pennsylvania 19083
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Philadelphia, PA
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800 Spruce St
Philadelphia, Pennsylvania 19107
215-829-3000
Pennsylvania Hospital Pennsylvania Hospital, the nation's first hospital, has been a leader in patient care,...
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Philadelphia, PA
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Redbank, New Jersey 07701
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Redbank, NJ
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Savannah, Georgia 31405
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Savannah, GA
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Springfield, Missouri 65807
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Springfield, MO
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Tacoma, Washington 98405
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from
Tacoma, WA
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Toms River, New Jersey 08755
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Toms River, NJ
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