SpineTRACK Registry - Spinal Outcomes Registry

SpineTRACK (Translating Radiographic and Clinical Knowledge) Registry: Outcomes Data Collection in Degenerative, Deformity, and Trauma Patients

The Spine TRACK Spinal Surgery Registry is a prospective multi-center observational data collection initiative, to capture clinical and radiographic outcomes in candidates for spine surgery with degenerative, deformity, and traumatic pathologies. As an observational database, there are no initial driving hypotheses, but rather data will be mined to answer unforeseen questions, but which may include broad topics such as comparative effectiveness between and among various surgical treatment options, and/or outcomes in various subgroups of patients such as defined by demographics, comorbidities, indications and symptoms, treatment variables, and/or outcome variables.

Study Overview

• Status: Completed
• Conditions: Spinal Deformity; Spinal Trauma; Vertebra; Degeneration
• Intervention / Treatment: Procedure: Surgery

• Study Type: Observational
• Enrollment (Actual): 8079

Contacts and Locations

Study Locations

• Brazil
  • Minas Gerais, Brazil
    • Hospital Ortopedico
  • BR
    • São Paulo, BR, Brazil
      • Luis Pimenta, MD
• United States
  • Arizona
    • Phoenix, Arizona, United States, 85251
      • Spine Group Arizona
  • California
    • La Jolla, California, United States, 92037
      • SD Center for Spinal Disorders
    • Orange, California, United States, 92868
      • Orthopaedic Specialty Institute
    • San Francisco, California, United States, 94143
      • UCSF Dept. of Orthopaedic Surgery
  • Colorado
    • Durango, Colorado, United States, 81301
      • Durango Orthopaedics
  • Florida
    • Tampa, Florida, United States, 33606
      • University of South Florida Department of Neurosurgery, Tampa General Hospital
  • Georgia
    • Atlanta, Georgia, United States, 30309
      • Piedmont Physicians
  • Illinois
    • Chicago, Illinois, United States, 60612
      • Midwest Orthopaedics at Rush University
  • Indiana
    • Indianapolis, Indiana, United States, 46278
      • OrthoIndy Northwest
  • Minnesota
    • Minneapolis, Minnesota, United States, 55454
      • University of Minnesota Medical
  • Missouri
    • Jefferson City, Missouri, United States, 65101
      • Spine Midwest
    • St Louis, Missouri, United States, 63128
      • Spinemore, LLC
  • Nevada
    • Las Vegas, Nevada, United States, 89109
      • Western Regional Center for Brain & Spine Surgery, Surgery Center of S. Nevada
  • New Jersey
    • Tomas River, New Jersey, United States, 08755
      • Ocean Orthopaedics
  • New York
    • Buffalo, New York, United States, 14203
      • University of Buffalo
  • North Carolina
    • Eden, North Carolina, United States, 27288
      • Morehead NeuroSpine
    • Raleigh, North Carolina, United States, 27609
      • Bone & Joint Surgery Clinic
    • Raleigh, North Carolina, United States, 27610
      • Wake Orthopaedics
  • Oregon
    • Eugene, Oregon, United States, 97401
      • NeuroSpine Institute
    • Medford, Oregon, United States, 97504
      • Team2 Solutions, LLC
  • Pennsylvania
    • Pittsburgh, Pennsylvania, United States, 15213
      • University of Pittsburgh Medical Center
  • Texas
    • Houston, Texas, United States, 77030
      • Houston Methodist Orthopedics & Sports Medicine
    • Lakeway, Texas, United States, 78738
      • Austin Spine
  • Utah
    • Salt Lake City, Utah, United States, 84124
      • Salt Lake Orthopedic Clinic
  • Washington
    • Puyallup, Washington, United States, 98372
      • NeoSpine
    • Spokane, Washington, United States, 99208
      • Northwest Orthopaedic Specialists, PS

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Child; Adult; Older Adult
• Accepts Healthy Volunteers: No

• Sampling Method: Probability Sample

Study Population

All patients who are evaluated and scheduled to undergo surgical treatment for a spine-related condition are eligible to participate in this registry.

Description

Inclusion Criteria:

• Candidate for spinal surgery

Study Plan

How is the study designed?

Number of groups / cohorts

3

Cohorts and Interventions

Group / Cohort	Intervention / Treatment
Degenerative; Patients being treated for degenerative spine conditions.	Procedure: Surgery; Patients will receive standard of care surgical treatment dependent on his/her spinal condition.
Deformity; Patients being treated for a deformity spine condition.	Procedure: Surgery; Patients will receive standard of care surgical treatment dependent on his/her spinal condition.
Trauma; Patients being treated for a trauma related spine condition.	Procedure: Surgery; Patients will receive standard of care surgical treatment dependent on his/her spinal condition.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
To create a database of radiographic and clinical outcome measures of spinal surgery patients to evaluate the efficacy of various procedures for multiple diagnoses.	24 months then annually thereafter

Collaborators and Investigators

• Sponsor: NuVasive
• Investigators: Study Director: Kyle Malone, MS, NuVasive

Publications and helpful links

Helpful Links

• Related Info

Study record dates

Study Major Dates

• Study Start: March 1, 2011
• Primary Completion (Actual): December 6, 2016
• Study Completion (Actual): December 6, 2016

Study Registration Dates

• First Submitted: March 25, 2011
• First Submitted That Met QC Criteria: June 10, 2011
• First Posted (Estimated): June 14, 2011

Study Record Updates

• Last Update Posted (Estimated): December 24, 2025
• Last Update Submitted That Met QC Criteria: December 17, 2025
• Last Verified: December 1, 2025

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Congenital Abnormalities; Surgical Procedures, Operative
• Other Study ID Numbers: NUVA.REG1101

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO