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Kyphosis clinical trials

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NCT ID: NCT04125147 Terminated - Clinical trials for Ankylosing Spondylitis

Clinical Investigation of MONTAGE in Adults With Spinal Deformity Undergoing Pedicle Subtraction Osteotomy

Start date: December 5, 2019
Phase: N/A
Study type: Interventional

This study evaluates the difference in postoperative bleeding between two study groups, FDA cleared MONTAGE Settable Resorbable Hemostatic Bone Putty and standard of care (no bone hemostat) during pedicle subtraction osteotomy procedures.

NCT ID: NCT02411799 Terminated - Spinal Stenosis Clinical Trials

Instrumented Thoracic and Lumbar Arthrodesis Supplemented by the Implanet Jazz SystemTMd

Start date: April 2015
Phase:
Study type: Observational [Patient Registry]

Establish a data repository of patients who have undergone thoracic and/or lumbar instrumented arthrodesis procedure supplemented by the Implanet Jazz System.

NCT ID: NCT01852747 Terminated - Scoliosis Clinical Trials

Comparison of Actifuse ABX and Local Bone in Spinal Surgery

Start date: March 2013
Phase: Phase 4
Study type: Interventional

This study is being done to compare people who had a standard of care spinal fusion using part of their local bone graft (a small amount of bone from the region of the spine where the fusion is occurring) to correct an adult spinal deformity and people who will have a standard of care spinal fusion using a mixture of Actifuse ABX® (a market approved bone graft substitute) and a local bone graft (a small amount of bone from the region of the spine where the fusion is occurring). This study will compare the outcomes of both groups to help the Orthopaedic surgeon conducting spinal fusions in the future. Investigators expect that Actifuse ABX® will be as good if not better than just a local bone graft.

NCT ID: NCT01461005 Terminated - Spondylolisthesis Clinical Trials

A Postmarket Surveillance Study of the Paradigm Spine Dynamic Stabilization System (DSS)

DSS
Start date: September 2011
Phase: N/A
Study type: Interventional

The purpose of the Post-Market Surveillance study is to evaluate safety.

NCT ID: NCT00640029 Terminated - Kyphosis Clinical Trials

Evaluation of the Prosthetic Disc Replacement

EVA
Start date: February 2008
Phase: N/A
Study type: Interventional

Until now, arthrodesis (intervertebral fusion) is the formal treatment for the lumbar and cervical degenerative disc disease : arthrodesis has been the standard surgical treatment for the patients when nonsurgical management has failed. However , it has shown out some drawbacks : pseudoarthrosis may appear in the short term, and junctional degeneration in the long term. The replacement of the intervertebral disc by a prosthesis (arthroplasty) has been since a few years a major alternative therapeutic to the arthrodesis.: it demonstrates great functional results and less post-interventional complications. It is indicated to restore a normal function of the spine (motion is kept)and to avoid deterioration of the adjacent spinal segments over the long time. In this clinical study, we will distinguish the cervical discal pathology and the lumbar discal pathology. The purpose of this study is to analyze the results of the arthroplasty in terms of functional effects, quality of life, anatomical results and economical results.