OrthoTRACK Registry

A simple tool to track patients’ recovery progress and help contribute to improving the future of joint arthroplasty

OrthoTRACK™ Registry Brochure

The OrthoTRACK™ (Translating Radiographic and Clinical Knowledge) Registry is a prospective, multicenter, observational quality improvement tool. The platform allows participants to collect comprehensive treatment and outcomes data on patients undergoing joint arthroplasty procedures,* regardless of treatment or products used.

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Patients

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

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Participants

Use real-time reports to assess treatment outcomes

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Hospitals

Evaluate variation in outcomes to gain insight into the overall quality of care

The OrthoTRACK™ Registry provides:

  • Simple and intuitive data entry
  • Securely hosted and HIPAA-compliant browser-based platform
  • Smartphone- and tablet-friendly use with 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 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 OrthoTRACK™ Registry, please contact clinicalaffairs@globusmedical.com.

Frequently Asked Questions

Who can participate in the OrthoTRACK™ 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 OrthoTRACK™ implementation.

Is this tool available globally?

The OrthoTRACK™ Registry is currently only available in the United States.

What is the process to join the OrthoTRACK™ 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 formal training are required before access to the registry platform can be granted.

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*Scope expansion to include limb lengthening and trauma is underway.