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Kineflex Artificial Disc System to Treat Degenerative Disc Disease (DDD)

NCT00292292 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 514

Last updated 2013-09-13

No results posted yet for this study

Summary

The Kineflex Spinal System is no worse than the Charite Spinal System in patients with single level degenerative disc disease at L4/5 or L5/S1.

Conditions

  • Degenerative Disc Disease

Interventions

DEVICE

Lumbar Artificial Disc

Insertion of the Kineflex Lumbar ArtificialDisc

DEVICE

Charite Artificial Disc

Insertion of the Charite

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
2005-01-31
Primary Completion
2009-05-31
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 NCT00292292 on ClinicalTrials.gov