Clinical trial Recruiting at 2 sites Observational

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.

More Neoplasms trials

Quick facts

Study typeObservational
SexAll
Enrollment50000 (estimated)
SponsorThe Radiosurgery Society
Academic / other
Drugs / interventionsRadiation
Locations13 sites (Colorado Springs, Colorado and 12 other locations)
StatusRecruiting
StartedMarch 2012
Main results expectedDecember 2030
Study endsDecember 2030
Registry record updatedSeptember 19, 2024
Trial IDNCT01885299 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

  • 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
  • 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.