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Bone Graft Materials Observational Registry

NCT00974623 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 329

Last updated 2017-04-05

No results posted yet for this study

Summary

A multi-center, prospective, observational patient registry to collect information on the clinical outcomes and "real world" use of approved and commercially available bone graft substitutes, autograft and allograft.

Conditions

  • Degenerative Disc Disease
  • Herniated Disc
  • Spinal Stenosis
  • Spondylolithesis
  • Spinal Deformity
  • Cervical Myelopathy
  • Failed Back Surgery Syndrome
  • Spinal Cord Neoplasms

Interventions

DEVICE

Bone graft substitute, autograft or allograft

spine fusion surgery utilizing any commercially available bone graft substitute(s), autograft or allograft

Sponsors & Collaborators

  • Apatech, Inc.

    collaborator INDUSTRY

  • Baxter Healthcare Corporation

    lead INDUSTRY

Principal Investigators

  • Huub Kreuwel, Ph.D · Director of Medical Affairs

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-09-30
Primary Completion
2013-01-31
Completion
2013-11-30

Countries

  • United States
  • Hungary
  • Netherlands

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00974623 on ClinicalTrials.gov