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Kineflex|C Artificial Disc System to Treat Cervical Degenerative Disc Disease (DDD)

NCT00374413 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 343

Last updated 2013-09-13

No results posted yet for this study

Summary

The purpose of this study is to show that the Kineflex\|C Spinal System is no worse than conventional Anterior Cervical Diskectomy with Fusion (ACDF) in patients with single level degenerative disc disease at any cervical level from C3 to C7.

Conditions

  • Degenerative Disc Disease (DDD)

Interventions

DEVICE

Artificial disk

Implant

DEVICE

Artificial disc

Implant

Sponsors & Collaborators

  • SpinalMotion

    lead INDUSTRY

Principal Investigators

  • Fred Geisler, MD · Medical Monitor

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-07-31
Primary Completion
2010-01-31
Completion
2013-08-31

Countries

  • United States

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 NCT00374413 on ClinicalTrials.gov