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Spondylosis clinical trials

View clinical trials related to Spondylosis.

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NCT ID: NCT02023372 Completed - Spinal Stenosis Clinical Trials

Efficacy Study of NuCel® in Patients Undergoing Fusion of the Lumbar Spine

Start date: December 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether NuCel is effective in promoting spinal fusion in degenerative disease of the lumbar spine.

NCT ID: NCT02018445 Completed - Stenosis Clinical Trials

Accell Evo3™ Demineralized Bone Matrix in Instrumented Lumbar Spine Fusion

Start date: November 2013
Phase: N/A
Study type: Interventional

The objective of this study is to prospectively evaluate the performance of Integra Accell Evo3 Demineralized Bone Matrix as an adjunct for instrumented posterolateral spine fusion, as compared to local autograft.

NCT ID: NCT02005081 Recruiting - Clinical trials for Cervical Spondylosis With Myelopathy

Baxter: Actifuse SHAPE vs DBX in ACC

Start date: October 2013
Phase: N/A
Study type: Interventional

The purpose of this single-center, prospective, randomized study is to determine the fusion rates along with the clinical outcomes of commercially available bone graft substitutes Actifuse mixed with bone marrow aspirate (BMA) versus autograft mixed with demineralized bone matrix (DBM), in subjects who require anterior cervical corpectomy (ACC) spinal fusion in patients experiencing cervical spondylotic myelopathy (CSM).

NCT ID: NCT01918943 Recruiting - Low Back Pain Clinical Trials

Evaluation of Aspen Spinous Process Fixation System and PLIF Technique for the Treatment of Low Back Pain

Start date: August 2012
Phase: N/A
Study type: Observational

Lumbar spinal fusion was introduced approximately 70 years ago and has evolved as a treatment option for symptomatic spinal instability, spinal stenosis, spondylolisthesis, and degenerative scoliosis. Many techniques evolved since then, from wiring, rods, pedicle screws, and recently inter-spinous fixation devices like the Aspen. Along its evolutionary trail, various methods for achieving circumferential fusion have arisen. Distinct from staged anterior/posterior fusion techniques, two methods of achieving an interbody fusion from a posterior approach have emerged: posterior lumbar interbody fusion (PLIF) and transforaminal lumbar interbody fusion (TLIF). Recently, the lateral approach for interbody fusion (XLIF) has became a more common technique, requiring in some cases, complemental posterior fixation with pedicle screws, facet screws or interspinous fixation devices like the Aspen device. In this study, we address the clinical and radiological outcome of a novel technique using standard PLIF interbody fusion and insertion of the Aspen device via posterior lumbar approach.

NCT ID: NCT01873586 Completed - Stenosis Clinical Trials

OsteoStrux™ Collagen Ceramic Scaffold in Instrumented Lumbar Spine Fusion

Start date: October 2012
Phase: N/A
Study type: Interventional

The objective of this study is to prospectively evaluate the performance of Integra's OsteoStrux Collagen Ceramic Scaffold combined with bone marrow aspirate as an adjunct for instrumented posterolateral spine fusion, as compared to local autograft.

NCT ID: NCT01868958 Completed - Clinical trials for Cervical Spondylosis With Myelopathy

DTI of the Brain and Cervical Spine: Evaluation in Normal Subjects and Patients With Cervical Spondylotic Myelopathy

Start date: January 2013
Phase: N/A
Study type: Observational

More than half of the middle-aged population has radiologic evidence of cervical spondylosis (Irvine 1965) and a subset of this population develops cervical spondylotic myelopathy (CSM), a condition in which the spinal cord is impaired, either by direct mechanical compression or indirectly by arterial deprivation and/or venous stasis. In this study we aim to test the hypothesis that diffusion tensor imaging can provide prognostic information on the integrity of the spine in these patients which is unavailable from conventional MRI images

NCT ID: NCT01714804 Completed - Stenosis Clinical Trials

Efficacy and Safety of Integra Accell Evo3 DBM in Instrumented Lumbar Spine Fusion

Start date: August 2012
Phase: N/A
Study type: Interventional

The objective of this study is to prospectively evaluate the performance of Integra Accell Evo3 Demineralized Bone Matrix as an adjunct for instrumented lumbar spine fusion with a retrospective comparison to a historical patient cohort.

NCT ID: NCT01616719 Withdrawn - Clinical trials for Cervical Radiculopathy

Evaluation of DTRAX Graft in Patients With Cervical Degenerative Disc Disease

Start date: May 2012
Phase: N/A
Study type: Interventional

DTRAX Graft is used to relieve nerve pressure in the neck in order to provide relief for Cervical Degenerative Disc Disease. This study is being conducted to determine the effectiveness of the graft, and to find out whether or not it provides better results or faster healing than traditional ways of performing surgery for Cervical Degenerative Disc Disease.

NCT ID: NCT01603836 Completed - Clinical trials for Spondyloarthrosis, Spondylosis

Study Confirms or Refutes the Hypothesis That the Autologous Bone Marrow Concentrate Together With the Allograft is a Better Alternative for the Posterolateral Fusion in Spine Surgery Than the Allograft Alone

Start date: February 2009
Phase: N/A
Study type: Interventional

The use of autologous mesenchymal stem cell (MSCs) in form of the BMC in combination with allograft is an effective option how to enhance the Posterolateral Fusion (PLF) healing. Allograft by itself is not an effective material as a posterior onlay graft for the PLF in adult surgery.

NCT ID: NCT01430299 Completed - Stenosis Clinical Trials

Efficacy and Safety of Accell Evo3 Demineralized Bone Matrix (DBM) in Instrumented Posterolateral Lumbar Spine Fusion

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

The objective of this study is to prospectively evaluate the performance of Integra Accell Evo3 Demineralized Bone Matrix as an adjunct for posterolateral spine fusion with a retrospective comparison to a historical patient cohort.