CClinicalTrials.gg
CompletedNCT01372592Updated Dec 24, 2025

SpineTRACK Registry - Spinal Outcomes Registry

An observational study in Vertebra; Degeneration, Spinal Trauma and Spinal Deformity, sponsored by NuVasive. Completed at 28 sites in 2 countries. Per ClinicalTrials.gov, last updated 2025-12-24.

Sponsored by NuVasive · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
8,079
Sex
All
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Study summary

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.

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Conditions studied

  • Vertebra; Degeneration
  • Spinal Trauma
  • Spinal Deformity
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In context

Lead sponsor

NuVasive is the lead sponsor of 38 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
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.

Eligibility criteria

Inclusion Criteria:

  • Candidate for spinal surgery
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
8,079 participants (actual)

Groups and cohorts

  • Degenerative

    Patients being treated for degenerative spine conditions.

    Procedure: Surgery

  • Deformity

    Patients being treated for a deformity spine condition.

    Procedure: Surgery

  • Trauma

    Patients being treated for a trauma related spine condition.

    Procedure: Surgery

Interventions

  • ProcedureSurgery

    Patients will receive standard of care surgical treatment dependent on his/her spinal condition.

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What researchers measure

Primary outcomes

  1. To create a database of radiographic and clinical outcome measures of spinal surgery patients to evaluate the efficacy of various procedures for multiple diagnoses.

    Time frame: 24 months then annually thereafter

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Study locations

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

Related links

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 24, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01372592
Lead sponsor
NuVasive
Responsible party
Sponsor
First posted
Jun 14, 2011
Start date
Mar 2011
Primary completion
Dec 6, 2016
Completion
Dec 6, 2016
Last update
Dec 24, 2025

Study contacts

Kyle Malone, MS
study director · NuVasive

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2025. You cannot join it, but the record below documents what was studied.

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