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Clinical trial

Lumbar Interbody Fusion Using The Telamon® Peek™ Versus The Telamon® Hydrosorb™ Fusion Device - A Prospective, Randomized Controlled Trial To Assess Surgical And Clinical Outcomes

NCT00095095 is registered in ClinicalTrials.gov with Medtronic Spinal and Biologics as lead sponsor.

NCT NCT00095095
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Registry record

As filed in ClinicalTrials.gov.

Title
Lumbar Interbody Fusion Using The Telamon® Peek™ Versus The Telamon® Hydrosorb™ Fusion Device - A Prospective, Randomized Controlled Trial To Assess Surgical And Clinical Outcomes
Lead sponsor
Medtronic Spinal and Biologics
Phase
Phase 4
Overall status
Terminated
Start date
October 31, 2004
Completion date
May 31, 2006
Enrollment
102
Sites
4

Conditions

As the registry lists them; a condition with its own page is linked.

intervertebral disc displacement, low back pain, spinal stenosis, spondylolisthesis