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Completed Not applicable Interventional Results available

INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clinical Trial

ClinicalTrials.gov ID: NCT00485173

Public ClinicalTrials.gov record NCT00485173. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 12:05 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Pivotal Clinical Investigation of INFUSE® Bone Graft With a PEEK Interbody Spacer and an Anterior Cervical Plate in Patients With Cervical Degenerative Disc Disease at a Single Level.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the safety and effectiveness of the investigational implant (INFUSE® Bone Graft/PEEK Interbody Spacer/Anterior Cervical Plate) as a method of facilitating spinal fusion at a single level from C3-C7 in patients with symptomatic cervical degenerative disc disease.

Study identification

NCT ID
NCT00485173
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Medtronic Spinal and Biologics
Industry
Enrollment
224 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 2007 (Type not available)
Primary completion
Dec 2011 (Actual)
Completion
Jun 2012 (Actual)
Last update posted
Mar 19, 2013

2007 – 2012

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
S & B Surgery Center Beverly Hills California 90210 —
Orange County Neurological Association Laguna Hills California 92653 —
Crane Creek Medical Ctr. The Back Center /Osler Medical Melbourne Florida 32901 —
The Hughston Clinic, P.C. Columbus Georgia 31908 —
University of Kansas Medcal Center Kansas City Kansas 66160 —
Spine Institute Shreveport Louisiana 71103 —
Springfield Neurological Institute Springfield Missouri 65804 —
Buffalo Neurosurgery Group West Seneca New York 14224 —
University of Cincinnati Dept of Neurosurgery Cincinnati Ohio 45219 —
TriState Orthopedic Treatment Center Norwood Ohio 45212 —
The Washington Hospital Washington Pennsylvania 15301 —
Center for Sports Medcine & Orthopedics Chattanooga Tennessee 37404 —
Semmes Murphey Neurologic & Spine Institute Memphis Tennessee 38120 —
Central Texas Spine Austin Texas 78731 —
Brain and Spine Center of Texas, L.L.P. Plano Texas 75093 —
Inland Neurosurgery & Spine Associates, P.S. Spokane Washington 99204 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00485173, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 19, 2013 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00485173 live on ClinicalTrials.gov.

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