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Active clinical trials for "Spondylosis"

Results 91-100 of 112

The Effect of Midazolam Sedation on Diagnostic Medial Branch Blocks

Lumbar Spine SpondylosisAnxiety Generalized

This prospective observational study aims to investigate the effect of midazolam sedation on the diagnostic validity of diagnostic lumbar medial branch block in patients diagnosed with lumbar spondylosis without myelopathy.

Completed16 enrollment criteria

Medial Branch Radiofrequency Ablation and Lumbar Multifidi

SpondylosisOsteoarthritis

The purpose of this study is to evaluate the effects of lumbar medial branch radiofrequency ablation (RFA) on lumbar multifidi muscle size and clinical spinal stability. Specifically, this study is designed to highlight the comparison of multifidi muscle architecture using ultrasound imaging (USI) and MRI before and after lumbar medial branch RFA. This study will also include a commonly utilized functional assessment of the lumbar spine to evaluate the effects of RFA on lumbar spinal stability.

Completed13 enrollment criteria

UNiD 3D VBR Register

Spinal Cord CompressionSpondylosis4 more

Multicenter study allowing to include the first sixty patients implanted with a custom-made corpectomy implant (UNiD 3D VBR): 30 patient implanted in cervical region and 30 patients implanted in thoracolumbar region. The main objective is to confirm feasibilty and safety of patient-specific implants for one or multi-level corpectomy and fusion. This study was approved in March 2016 allowing to include retrospectivley all patients since the first implantation in January 2015 and prospectively all patients after the approval.

Completed26 enrollment criteria

An ACDF Multi-Center Study Using ViviGen Cellular Bone Matrix

Cervical SpondylosisDegenerative Intervertebral Discs1 more

The purpose of this post-market study is to collect data on ViviGen and how its use affects fusion rates in the cervical spine when used as additional grafting material to fill the cervical spacer. The patient population of interest is patients who have already elected to undergo a 2-3 level ACDF surgical procedure using ViviGen, per standard of care.

Completed29 enrollment criteria

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

Spinal Cord InjuryCervical Spondylosis With Myelopathy1 more

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.

Completed26 enrollment criteria

Protection of Autonomic Nervous System During Lower Spine Surgical Procedures: A Safety and Feasibility...

Intervertebral Disc DegenerationIntervertebral Disc Displacement7 more

A safety and feasibility study of free-run and stimulated corporal electromyography (EMG) to assess autonomic neural function during spinal and/or pelvic surgery in women and men.

Unknown status6 enrollment criteria

Retest-reliability and At-home-assessment Feasibility of the 5R-STS

Degenerative Disc DiseaseSpondylolisthesis5 more

The five-repetition sit-to-stand test has been validated and is used primarily in pulmonary medicine and cardiology, and has recently been shown to be a useful tool for the objective assessment of functional impairment in patients with degenerative diseases of the lumbar spine. The goal of this study is to assess the possibility of supervised and unsupervised at-home-assessment. Validation of at-home-assessment would allow the 5R-STS to be easily used as a follow-up tool in clinical trials, for example.

Completed4 enrollment criteria

ViBone in Cervical and Lumbar Spine Fusion

SpondylosisCervical Spondylosis3 more

Assess clinical and radiographic outcomes in patients who undergo 1-3 level anterior cervical discectomy fusion (ACDF) or lumbar interbody fusion (TLIF, PLIF, ALIF, or LLIF) using ViBone.

Completed18 enrollment criteria

Cost Effectiveness of OMT for Chronic Low Back Pain

Lumbar RadiculopathyLesion of Sciatic Nerve9 more

The specific aim of this study is to conduct a prospective, multicenter cohort study over four months to compare the cost of standard of allopathic care (control group, N=90) versus standard of care plus osteopathic manipulative treatment (experimental group, N=90) in a cohort of 180 consecutive patients seeking treatment for chronic low back pain at three osteopathic clinics and three allopathic medical clinics (offering only standard care) located in three different regions of the United States.

Completed11 enrollment criteria

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

DegenerationSpondylosis2 more

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

Completed2 enrollment criteria
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