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Degenerative Lumbar Disc Disease clinical trials

View clinical trials related to Degenerative Lumbar Disc Disease.

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NCT ID: NCT02272140 Completed - Clinical trials for Degenerative Lumbar Disc Disease

Advanced XLIF Monitoring Multicenter Study

Start date: July 9, 2014
Phase:
Study type: Observational

The objective of this study is to evaluate the utility of localized stimulation of the lumbosacral nerve roots during XLIF through correlation of observed changes in the response latency, amplitude, waveform morphology, and/or response threshold with surgical events. Additionally, correlation between neuromonitoring findings and postoperative neural status will be evaluated.

NCT ID: NCT02192112 Completed - Clinical trials for Degenerative Lumbar Disc Disease

Advanced XLIF Monitoring Pilot Study

Start date: June 2014
Phase:
Study type: Observational

Though the utility of NVM5 neuromonitoring by stimulating within the surgical site during XLIF has been demonstrated, it is hypothesized that more information may be gathered if a greater section of the motor neural pathway was monitored (i.e., stimulation above the surgical site and recording the subsequent muscle response in the lower limbs). Currently, there has not been demonstrated a practical method of stimulating the lumbosacral nerve roots locally, but well-above the surgical site in this fashion. This protocol is intended to evaluate the feasibility and reproducibility of using surface stimulation and return (anode) electrodes to stimulate the lumbosacral nerve roots, and record responses from the relevant innervated muscle groups of the lower limbs.

NCT ID: NCT00493558 Completed - Spinal Stenosis Clinical Trials

Spine Research With Roentgen Stereophotogrammetric Analysis

SpineRSA
Start date: July 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to gather information on the effectiveness of a new spine implant for patients who require spinal fusion surgery. Based on this information, we hope to create a standard of good performance, or benchmark, against which future studies on this spine implant can be compared. By creating this benchmark we hope to improve care for patients who require spinal fusion surgery.

NCT ID: NCT00405600 Completed - Spinal Stenosis Clinical Trials

Spine Fusion Instrumented With BMP-2 vs Uninstrumented With Infuse BMP-2 Alone

Start date: November 2006
Phase: N/A
Study type: Interventional

The goal of spinal fusion is to relieve pain and/or increase stability in painful or unstable spine joints. A patient may or may not receive rods and screws with the use of bone graft materials to facilitate bone growth and a fusion thus preventing movement of the bones of the spine. In this research study, bone graft substitute material called Bone Morphogenetic Protein-2 known as BMP-2 Infuse will be used. No hip bone will be used. The surgical procedure will consist of BMP-2 Infuse with or without the use of rods and screws.