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Spondylosis clinical trials

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NCT ID: NCT01407705 Completed - Spinal Cord Injury Clinical Trials

High-Resolution Diffusion Tensor Imaging (DTI) of the Cervical Spinal Cord in the Setting of Spinal Cord Injury (SCI)

Start date: May 2007
Phase: N/A
Study type: Observational

The investigators propose a prospective study, designed to analyze the efficacy of High-Resolution Diffusion Tensor Imaging for accurately sensing white matter tracts in subjects with spinal cord injury. Study subjects will not be randomized, as treatment will follow the doctor's "standard of care." Patients will be selected and offered enrollment based upon the clinical diagnosis of spinal cord injury, either due to degenerative disease or trauma. Enrollment will be based on the chronology of patient presentation.

NCT ID: NCT01383876 Terminated - Clinical trials for Cervical Spondylosis Symptomatic Neurological Compression

Collar Immobilization Following a Posterior Cervical Laminectomy and Fusion

Start date: June 2011
Phase: N/A
Study type: Interventional

Cervical collars are commonly used to provide external immobilization after elective Posterior Cervical Laminectomy and Interbody Fusion (PCLIF). The rationale for collar use is the perception and assumption that it can prevent early instrumentation failure and promote successful spinal fusion. However, there are a number of potential complications associated with cervical collars such as skin breakdown, ulceration, neck pain, impedance upon activities of daily living, and impaired swallowing. Considering these conflicting factors, there is wide disagreement among spinal surgeons about the utility, benefits, and necessity of collar use following elective PCLIF. Hypothesis: Wearing a cervical collar for 12 weeks after posterior cervical laminectomy and instrumented fusion will not demonstrate substantial benefits as measured by the incidence of instrumentation failure, rate of nonunion, or clinical outcome measures. Specific Aim I: To compare the outcomes of surgery in patients who will wear a cervical collar for 12 weeks following surgery versus those who will have the collar removed prior to discharge after surgery.

NCT ID: NCT01292252 Completed - Clinical trials for Lumbar Spondylolisthesis

Use of Forteo (Teriparatide) in Posterolateral Lumbar Spine Fusion

Start date: August 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effects of 12 weeks of daily treatment with teriparatide on spine fusion in adult patients who are undergoing multi-level posterolateral spine fusion surgery for degenerative conditions of the lumbar spine.

NCT ID: NCT01243684 Completed - Clinical trials for Cervical Spondylosis

A Magnetic Resonance Imaging Study of Patients With Cervical Spondylosis

Tractocervical
Start date: September 2010
Phase: N/A
Study type: Interventional

This study aims at evaluating spinal cord structure using diffusion tensor imaging in patients with cervical spondylosis.

NCT ID: NCT01061697 Completed - Clinical trials for Cervical Spondylosis

Pregabalin and Radicular Pain Study (PARPS)

PARPS
Start date: January 2008
Phase: Phase 4
Study type: Interventional

This study is designed to investigate the effectiveness of pregabalin (Lyrica) on nerve pain caused by degenerative neck problems. Pregabalin is a new drug registered for use in nerve pain worldwide

NCT ID: NCT00788008 Completed - Knee Osteoarthritis Clinical Trials

Cognitive Effects of Inhalational Versus Intravenous General Anesthesia in the Elderly

Start date: November 2008
Phase: N/A
Study type: Interventional

The purpose of this research is to determine if post-operative cognition will be better if the general anesthesia for surgery is done with an inhaled (gas through a breathing tube) or intravenous (medicine injected in the IV) general anesthetic technique.

NCT ID: NCT00555659 Completed - Stenosis Clinical Trials

Prospective Clinical Evaluation of the New Aegis Plate for Anterior Interbody Fusions

Aegis
Start date: September 2007
Phase: N/A
Study type: Observational

Introduction: Degenerative changes of the discs and facet joints in the lumbar spine can result in pain and disability from spondylosis, spondylolisthesis and stenosis. Patients who are suffering with back and/or leg pain are potential candidates for an ALIF procedure. Purpose: To assess and compare clinical outcomes and fusion rates in patients undergoing an instrumented ALIF procedure. Comparisons in all variables will be made across diagnostic categories. Comparisons between type of interbody spacer, graft type, and type of instrumentation will also be made