Long-term tracking of Stereotactic Radiosurgery and Stereotactic Body Radiation Therapy use
Official title: Multi-Institution Registry of SRS/SBRT Procedures
Run by The Radiosurgery Society · NCT01885299 · Data updated 2026-11-12
This study is tracking how well Stereotactic Radiosurgery and Stereotactic Body Radiation Therapy work for treating tumors over time to help improve patient care.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 50000 (estimated) |
| Sponsor | The Radiosurgery Society Academic / other |
| Drugs / interventions | Radiation |
| Locations | 13 sites (Colorado Springs, Colorado and 12 other locations) |
| Status | Recruiting |
| Started | March 2012 |
| Main results expected | December 2030 |
| Study ends | December 2030 |
| Registry record updated | September 19, 2024 |
| Trial ID | NCT01885299 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include patients diagnosed with benign or malignant tumors or other conditions treatable by SRS/SBRT.
✕Probably not a fit
Patients who are unwilling to sign the informed consent document will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The RSSearch Registry is an international database that collects data on the use of Stereotactic Radiosurgery (SRS) and Stereotactic Body Radiation Therapy (SBRT) for treating various tumors and conditions. It aims to track treatment practices and outcomes over time, allowing healthcare providers to analyze the effectiveness of these therapies. Participants can record patient characteristics, treatment plans, and outcomes, facilitating quality improvement and collaboration among treatment centers. The registry also includes both prospective enrollment and retrospective data to capture comprehensive treatment outcomes.
Why it matters
Potential benefit: If successful, this registry could enhance the understanding and effectiveness of SRS/SBRT treatments, leading to improved patient outcomes.
How similar studies have gone: Other studies utilizing registries for tracking treatment outcomes have shown success, indicating that this approach is both tested and valuable.
Who can join: the full rules
Show full inclusion / exclusion 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
Where it's running
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Sylvester Comprehensive Cancer Center, University of Miami
Miami, Florida, United States Recruiting -
Henry Ford Health System
Detroit, Michigan, United States Recruiting -
Penrose Cancer Center
Colorado Springs, Colorado, United States Enrolling by invitation -
Southeast Georgia Health System
Brunswick, Georgia, United States Enrolling by invitation -
AtlantiCare Regional Medical Center and AtlantiCare Cancer Care Institute
Egg Harbor, New Jersey, United States Enrolling by invitation -
Riverview Medical Center
Red Bank, New Jersey, United States Enrolling by invitation
Show 7 more locations
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NJ Cyberknife at Community Medical Center
Toms River, New Jersey, United States Enrolling by invitation -
Montefiore Medical Center
The Bronx, New York, United States Enrolling by invitation -
Geisinger Health System
Danville, Pennsylvania, United States Enrolling by invitation -
Philadelphia CyberKnife
Philadelphia, Pennsylvania, United States Enrolling by invitation -
Pottstown Memorial Medical Center
Pottstown, Pennsylvania, United States Enrolling by invitation -
Cyberknife at Erlanger
Chattanooga, Tennessee, United States Enrolling by invitation -
St. Mary's Medical Center
Huntington, West Virginia, United States Enrolling by invitation
Study contacts
- Study coordinator: Jan Jenkins, RN
- Email: jjenkins@therss.org
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.