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Internal Disc Disruption clinical trials

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NCT ID: NCT01011816 Terminated - Back Pain Clinical Trials

Treatment of Symptomatic Lumbar Internal Disc Disruption (IDD) With the Biostat® System

Start date: March 2010
Phase: Phase 3
Study type: Interventional

The purpose of this investigation is to establish the safety and efficacy of the Biostat System when used for treatment of chronic low back (lumbar) pain due to symptomatic internal disc disruptions (IDD) by comparing safety and efficacy outcome measures between one group receiving BIOSTAT BIOLOGX® Fibrin Sealant through the Biostat® Delivery Device and another group receiving a preservative-free normal saline control delivered with the Biostat Delivery Device.