A simple tool to track patients’ recovery progress and help contribute to improving the future of spine surgery
SpineTRACK™ Registry BrochureThe SpineTRACK™ (Translating Radiographic and Clinical Knowledge) Registry is a prospective, multicenter, observational quality improvement tool. SpineTRACK™ is a platform for participants to collect comprehensive treatment and outcomes data on all patients with spinal pathology, regardless of treatment or products used.

Patients
Engage in tracking their progress to better understand the results of their treatment

Participants
Use real-time reports to assess treatment outcomes

Hospitals
Evaluate variation in outcomes to gain insight into the overall quality of care
The SpineTRACK™ Registry provides:
- Simple and intuitive data entry
- Securely hosted and HIPAA-compliant, browser-based platform
- Smartphone- and tablet-friendly use with a point-of-care app
- Role-based logins to allow stratified levels of access to data
Registry data can be used to:
- Benchmark patient outcomes
- Quantify length of stay, complications, and revisions across procedures
- Track patient satisfaction and other patient-reported outcomes
- Quantify efficiency and outcome metrics
To learn more about eligibility and participation in the SpineTRACK™ Registry, please contact clinicalaffairs@globusmedical.com.
Frequently Asked Questions
Who can participate in the SpineTRACK™ Registry?
Participants must meet eligibility requirements in order to participate. These include current or prior demonstration of data collection capability, such as employing a designated staff member to oversee the data collection effort.
Are there costs to participate?
There are no fees for a site to participate. The site is responsible for all costs related to SpineTRACK™ implementation.
Is this tool available globally?
The SpineTRACK™ Registry is currently only available in the United States.
What is the process to join the SpineTRACK™ Registry?
Following a vetting process by Globus Clinical Affairs to assess for eligibility, Clinical Affairs will work with the participating site to obtain the proper approvals (ethics/quality committee, as required). A Participation Agreement, Business Associate Agreement, and a formal training are required before access to the registry platform can be granted.
