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Radiculopathy, Cervical clinical trials

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NCT ID: NCT03023696 Recruiting - Clinical trials for Radiculopathy, Cervical

Can Prophylactic Foraminotomy Prevent C5 Palsy

Start date: June 2016
Phase: N/A
Study type: Interventional

C5 palsy (C5P) is a well-known, although rare complication of cervical spine decompression surgery. In severe forms, C5P causes debilitating upper extremity weakness involving the deltoids and/or biceps brachii muscles, ultimately diminishing these patients' quality of life. Furthermore, about half of patients with C5P present with sensory deficits and/or intractable pain in addition to the muscle weakness. Prophylactic bilateral foraminotomy at the C5 level during cervical decompression surgery has been studied recently with the hope that it will minimize the risk of developing a C5 nerve root palsy postoperatively. Although the current literature provides some support for this claim, there are insufficient data establishing this technique as a proven measure to reduce the incidence of C5P. In the present study, we seek to evaluate the effect of bilateral foraminotomy on postoperative C5P incidence rates. Bilateral foraminotomy has been correlated with a reduced risk of developing C5P following cervical decompression surgery, but an identical foraminotomy procedure has never been applied in a randomized manner to all qualifying patients in a study. Additionally, prophylactic foraminotomy has only been prospectively studied during laminoplasty. In the proposed study, bilateral foraminotomy will be randomized to patients receiving cervical decompression surgery (laminoplasty, laminectomy, fusion). This is a multicenter randomized trial, including the following sites: Cleveland Clinic, Columbia University Medical Center, and University of Southern California Spine Center. Patients undergoing cervical decompression surgery will be consented and enrolled if they meet the inclusion and exclusion criteria. Subsequently, incidence of C5P will be monitored to determine efficacy of prophylactic C5 bilateral foraminotomy during cervical decompression.

NCT ID: NCT02761928 Terminated - Spinal Stenosis Clinical Trials

Investigation of Hypermobility, Biomarkers, and Pain Generators in Chronic Pain Patients

Hypermoble
Start date: January 2016
Phase:
Study type: Observational

Observational study of axial spine pain and hyperflexibility. Patients will receive physical exam maneuvers (traditional straight leg raise, FABER, facet loading as well as Beighton's hypermobility score) and blood / urine / saliva collection. They will also be separated into pain groups based on their response to injections. A correlation between exam findings and procedure group will be measured.

NCT ID: NCT01911013 Active, not recruiting - Myelopathy Clinical Trials

A Study of Korean Society of Spine Surgery on the Outcomes of Anterior Cervical Discectomy and Fusion

Start date: September 1, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is firstly to determine the efficacy of cervical plate for anterior cervical discectomy and fusion using cervical cage, and secondly to investigate the determining factors for surgical outcomes.

NCT ID: NCT00735176 Completed - Clinical trials for Radiculopathy, Cervical

The Norwegian Cervical Arthroplasty Trial

NORCAT
Start date: September 2008
Phase: N/A
Study type: Interventional

The study will compare cervical arthroplasty with cervical discectomy and fusion, in the treatment of cervical radiculopathy. The 0-hypothesis is that there is no difference between the two methods, when comparing primary and secondary outcome variables.

NCT ID: NCT00129714 Completed - Clinical trials for Radiculopathy, Cervical

Westeinde Brachialgia Study

WEB
Start date: August 2003
Phase: N/A
Study type: Interventional

The Westeinde Brachialgia Study (WEB) is a randomized controlled trial to establish the effect of cervical collar or physiotherapy compared to a wait-and-see policy in patients with acute cervical radiculopathy.