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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 Jul 22, 2026, 1:35 AM 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

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

Interventions

  • PRESTIGE® LP Cervical Disc Device
  • ATLANTIS Anterior Cervical Plate Device

Device

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
Dec 31, 2004
Primary completion
Dec 31, 2007
Completion
May 31, 2014
Last update posted
Jun 5, 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 5, 2023 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00667459 live on ClinicalTrials.gov.

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