Clinical Trials Directory

Trials / Recruiting

RecruitingNCT01885299

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

Multi-Institution Registry of SRS/SBRT Procedures

Status
Recruiting
Phase
Study type
Observational
Enrollment
50,000 (estimated)
Sponsor
The Radiosurgery Society · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

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.)

Detailed description

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.

Conditions

Interventions

TypeNameDescription
RADIATIONSRS/SBRTIntervention varies by condition being treated.

Timeline

Start date
2012-03-01
Primary completion
2030-12-01
Completion
2030-12-01
First posted
2013-06-24
Last updated
2024-09-19

Locations

13 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01885299. Inclusion in this directory is not an endorsement.