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Terminated Phase 3 Interventional

A Clinical Study of the Dynesys(R) Spinal System

ClinicalTrials.gov ID: NCT00759057

Public ClinicalTrials.gov record NCT00759057. 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 21, 2026, 12:37 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 Clinical Study of the Dynesys(R) Spinal System As a Non-fusion Device for Spinal Stabilization

Study identification

NCT ID
NCT00759057
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Zimmer Biomet
Industry
Enrollment
399 participants

Conditions and interventions

Interventions

  • Posterior Pedicle Screw System Device

Device

Eligibility (public fields only)

Age range
20 Years to 80 Years
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
Feb 28, 2003
Primary completion
May 31, 2015
Completion
Nov 30, 2015
Last update posted
Jun 27, 2012

2003 – 2015

United States locations

U.S. sites
26
U.S. states
18
U.S. cities
26
Facility City State ZIP Site status
Scottsdale Spine Center Scottsdale Arizona 85251
Northwest NeuroSpecialists Tucson Arizona 85741
Cedars-Sinai Medical Center, The Spine Institute Los Angeles California 90048
Pacific Regional Neurosurgery Modesto California 95350
Denver Spine Center Denver Colorado 80218
Medical Faculty Associates - The George Washington University Washington D.C. District of Columbia 20037
Orthopedic Care & Sports Medicine Center Aventura Florida 33180
Peachtree Orthopaedic Clinic Atlanta Georgia 30342
Fort Wayne Orthopedic Fort Wayne Indiana 46804
Indiana University Neurosurgical Indianapolis Indiana 46202
Heartland Spine and Hand Center Overland Park Kansas 66211
Spine Specialty Center (SSC) Baton Rouge Louisiana 70810
Baltimore Neurosurgical Associates, PA Baltimore Maryland 21204
Orthopaedic Associates Towson Maryland 21204
Sports Medicine North Peabody Massachusetts 01960
Orthopedic Consultants, PA Edina Minnesota 55435
Manhattan Orthopaedics, PC New York New York 10021
SUNY Upstate Medical University Dept of Orthopedic Surgery Syracuse New York 13202
Triangle Orthopedic Associates Durham North Carolina 27704
Orthopaedic Spine Associates Eugene Oregon 97401
Dept. of Neurosurgery UPMC Presbyterian Pittsburgh Pennsylvania 15213-2582
Abington Hospital Willow Grove Pennsylvania 19090
SPINE Mt. Pleasant South Carolina 29464
College Station Neurosurgery College Station Texas 77845
Park Plaza Hospital Houston Texas 77004
SpineMark CRO at TBI Plano Texas 75093

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 NCT00759057, 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 27, 2012 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00759057 live on ClinicalTrials.gov.

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