The RSSearch™ Registry is an international multiplatform research and data sharing registry aimed at generating peer reviewed publications and increasing collaboration among the diverse clinical specialties, hospitals and industries participating in SRS and SBRT. Participation in RSSearch is aimed at using data to improve the quality of care and medical decision making, access to novel treatments and approaches for patients, and furthering the development and science of SRS/SBRT treatment. Eventually, Clinical and quality guidelines based on evidence-based approaches will emerge from the registry. To participate, IRB approval is required.
Benefits of participating in RSSearch include:
- Secure web-based patient management registry designed to serve an entire SRS/SBRT patient population
- Ability to better track patient follow-up
- Allows secure and real-time access to your patient information
- Generate a wide variety of standard and customized reports
- Easy access to your treatment and outcomes data for publication and presentation
- Access to aggregate data upon application
- HIPAA and EU compliant
Click here to view the flyer or for more information, please email Nalani Brown at nbrown@therss.org.
Requests for Aggregate Data
1. Case 2012-0508
The RSSearch™ Registry is powered by AdvertekSM
