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Cervical Spondylotic Myelopathy clinical trials

View clinical trials related to Cervical Spondylotic Myelopathy.

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NCT ID: NCT01257828 Completed - Clinical trials for Cervical Spondylotic Myelopathy

Efficacy of Riluzole in Surgical Treatment for Cervical Spondylotic Myelopathy (CSM-Protect)

CSM-Protect
Start date: March 2012
Phase: Phase 3
Study type: Interventional

CSM (Cervical spondylotic myelopathy) is the most common cause of spinal cord injury worldwide. While there is evidence from the recently completed SpineNet prospective study that surgical decompression is an effective treatment for CSM, it is clear that many patients have remaining neurological impairment. While surgery is relatively safe, approximately 3% of patients maintain a neurological problem. Given this background and data from preclinical models of non-traumatic and traumatic spinal cord injury, there is strong evidence to consider the potential benefit of adding a neuroprotective drug which aids in the treatment of patients with CSM whom are undergoing surgical decompression. Riluzole is FDA-approved for the treatment of amyotrophic lateral sclerosis, which has some similar clinical features to CSM. Riluzole is currently under investigation for traumatic spinal cord injury. Given this background, there is a strong basis to consider studying the potential neurological benefits of Riluzole as a treatment to surgical decompression in patients with CSM.

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: NCT00876603 Recruiting - Clinical trials for Cervical Spondylotic Myelopathy

Anterior Vs Posterior Procedures for Cervical Spondylotic Myelopathy: Prospective Randomized Clinical Trial

CSM
Start date: May 2001
Phase: N/A
Study type: Observational

There is no difference in surgical outcomes for patients suffering from cervical spondylotic myelopathy treated with anterior decompression and fusion or posterior cervical laminoplasty.

NCT ID: NCT00565734 Completed - Clinical trials for Cervical Spondylotic Myelopathy

Surgical Treatment of Cervical Spondylotic Myelopathy

Start date: November 2007
Phase: Phase 4
Study type: Observational

The primary purposes of this study are to compare anterior and posterior surgical approach in treatment of CSM ad to compare variations in treatment and outcomes of CSM worldwide.

NCT ID: NCT00506558 Completed - Clinical trials for Cervical Spondylotic Myelopathy

The CSM Trial: A Multicenter Study Comparing Ventral to Dorsal Surgery for Cervical Spondylotic Myelopathy

CSM
Start date: November 2006
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine the optimal surgical approach (ventral versus dorsal) for patients with multi-level cervical spondylotic myelopathy (CSM). There are no established guidelines for the management of patients with CSM, which slowly causes spinal cord injury in afflicted patients. This study aims to test the hypothesis that ventral surgery (decompressing the spinal cord from the front of the neck) and dorsal surgery (decompressing the spinal cord from the back of the neck) might differ in their overall outcome or major complication rate.

NCT ID: NCT00285337 Completed - Clinical trials for Cervical Spondylotic Myelopathy

Assessment of Surgical Techniques for Treating Cervical Spondylotic Myelopathy

CSM
Start date: December 2005
Phase: N/A
Study type: Observational

The primary purpose of this study is to compare anterior and posterior surgical approach in treatment of CSM in terms of surgical complications and neurological, functional, disease-specific and quality of life outcomes measures. Secondary aims are to quantify the amount of change pre and post-surgery concerning the same outcome measures; to determine if there are differences in outcomes between posterior surgical techniques (i.e. laminectomy with fusion or laminoplasty) and examine the relationship between baseline MRI and baseline and follow-up neurological and functional outcomes.