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

NCT01885299 · The Radiosurgery Society
In plain English

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Official title
Multi-Institution Registry of SRS/SBRT Procedures
About this study
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 Vision Tree, 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.
Eligibility criteria
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 or verbally agree to participation Exclusion Criteria: * There are no specific exclusion criteria, but patients who are unwilling to sign the ICD or who decline participation will not be included
Study design
Enrollment target: 50000 participants
Age groups: child, adult, older_adult
Timeline
Starts: 2012-03
Estimated completion: 2030-12
Last updated: 2024-09-19
Interventions
Radiation: SRS/SBRT
Primary outcomes
  • Overall survival (Up to 5 years)
Sponsor
The Radiosurgery Society · other
With: VisionTree
Contacts & investigators
ContactJan Jenkins, RN · contact · jjenkins@therss.org
ContactJoanne Davis, PHD · contact · jdavis@therss.org
InvestigatorAnand Mahadevan, MD · study_director, The Radiosurgery Society
All locations (13)
Penrose Cancer CenterEnrolling By Invitation
Colorado Springs, Colorado, United States
Sylvester Comprehensive Cancer Center, University of MiamiRecruiting
Miami, Florida, United States
Southeast Georgia Health SystemEnrolling By Invitation
Brunswick, Georgia, United States
Henry Ford Health SystemRecruiting
Detroit, Michigan, United States
AtlantiCare Regional Medical Center and AtlantiCare Cancer Care InstituteEnrolling By Invitation
Egg Harbor, New Jersey, United States
Riverview Medical CenterEnrolling By Invitation
Red Bank, New Jersey, United States
NJ Cyberknife at Community Medical CenterEnrolling By Invitation
Toms River, New Jersey, United States
Montefiore Medical CenterEnrolling By Invitation
The Bronx, New York, United States
Geisinger Health SystemEnrolling By Invitation
Danville, Pennsylvania, United States
Philadelphia CyberKnifeEnrolling By Invitation
Philadelphia, Pennsylvania, United States
Pottstown Memorial Medical CenterEnrolling By Invitation
Pottstown, Pennsylvania, United States
Cyberknife at ErlangerEnrolling By Invitation
Chattanooga, Tennessee, United States
St. Mary's Medical CenterEnrolling By Invitation
Huntington, West Virginia, United States
RSSearch Patient Registry-Long Term Study of Use of SRS/SBRT · TrialPath