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Completed Phase 3 Interventional Results available

Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cervical Fusion in Cervical DDD

ClinicalTrials.gov ID: NCT00667459

Public ClinicalTrials.gov record NCT00667459. 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 22, 2026, 11:05 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 Prospective, Multicenter, Controlled Clinical Trial of an Artificial Cervical Disc LP at a Single Level for Symptomatic Cervical Disc Disease

Brief summary

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

The purpose of this clinical trial is to evaluate the safety and effectiveness of the PRESTIGE® LP Cervical Disc as a method of treating patients with symptoms of cervical degenerative disc disease at a single level from C3-C4 to C6-C7.

Study identification

NCT ID
NCT00667459
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Medtronic Spinal and Biologics
Industry
Enrollment
280 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
Jan 2005 (Type not available)
Primary completion
Jan 2008 (Actual)
Completion
Jun 2014 (Actual)
Last update posted
Jun 6, 2023

2005 – 2014

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Emory Orthopaedics and Spine Center Atlanta Georgia 30329 —
The Hughston Clinic, P.C. Columbus Georgia 31908 —
Coeur d'Alene Spine and Brain, PLLC Coeur d'Alene Idaho 83814 —
Central Illinois Neuroscience Bloomington Illinois 61701 —
Indiana Spine Carmel Indiana 46032 —
OrthoIndy Indianapolis Indiana 46260 —
Cedar Neurological Surgeons, PC Cedar Rapids Iowa 52403 —
Sports Medicine North Peabody Massachusetts 01960 —
The Orthopaedic Center of St. Louis Chesterfield Missouri 63017 —
Springfield Neurological Institute Springfield Missouri 65804 —
Buffalo Neurosurgery Group West Seneca New York 14224 —
NeuroSpine Institute, LLC Eugene Oregon 97401 —
Clinical Trials for South Carolina Charleston South Carolina 29406 —
Chattanooga Orthopaedic Group Chattanooga Tennessee 37404 —
Brain and Spine Center of Texas, L.L.P. Plano Texas 75093 —
University of Virginia,Neurosurgery Department Charlottesville Virginia 22908 —

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 NCT00667459, 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 Jun 6, 2023 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00667459 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →