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Cervical Myelopathy clinical trials

View clinical trials related to Cervical Myelopathy.

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NCT ID: NCT03842072 Recruiting - Clinical trials for Cervical Radiculopathy

The Collar Post Anterior Cervical Spine Surgery Study

C-PASS
Start date: February 23, 2018
Phase: N/A
Study type: Interventional

The Anterior Cervical Discectomy and Fusion (ACDF) represents one of the most commonly performed spinal operations internationally, often in the context of symptomatic radiculopathy or myelopathy secondary to cervical degenerative disease. Approximately half of surgeons continue to prescribe a period of post-operative bracing with a cervical collar. However, there is currently no high quality evidence available to support the routine use of post-operative bracing after ACDF; further, braces are expensive and have been associated with a variety of local complications. In summary, the current lack of evidence, and lack of consensus amongst surgeons, regarding best practices in the use of post-operative bracing after ACDF, places the surgeon and the patient in a precarious position. Our randomized trial comparing the impact of 6 weeks of post-operative bracing with a rigid cervical collar vs. no post-operative bracing, on a variety of clinical and radiological outcomes, for adult patients with cervical radiculopathy and/or myelopathy undergoing single or multi-level ACDF.

NCT ID: NCT03695848 Completed - Cervical Myelopathy Clinical Trials

Prognostic Value of DTI and fMRI of Cervical Myelopathy

CSM
Start date: September 26, 2018
Phase:
Study type: Observational

Cervical myelopathy (CM) is one of the most common degenerative spinal cord disorders affecting older people. The progression of CM is insidious and the neurological decline can vary between patients. Surgical decompression is considered the most effective way to treat CM, however, it is not free from risk and the surgical outcome is not always satisfactory. The expected outcome of surgical intervention for CM remains a difficulty. There is a pressing need for a reliable and quantitative approach to predict surgical outcomes of CM and the precise prognosis. Previous studies have suggested a number of prognostic factors, such as age, duration of symptoms, pre-operative neurological status and abnormal MRI, but their prognostic value remains controversial. Recently, diffusion tensor imaging (DTI) and fMRI have been proposed as a promising tool for predicting the surgical prognosis of CM. In previous study, the protocol was successfully established for DTI microstructural characterization and resting state fMRI of the cervical spinal cord. This study is to evaluate the value of DTI and fMRI in predicting the outcome of surgical treatment. The ultimate goal is to establish a clinical protocol for quantitative DTI and fMRI analysis that could give accurate prognosis for surgical intervention to CM.

NCT ID: NCT03400644 Completed - Cervical Myelopathy Clinical Trials

Are Rigid Cervical Collars Necessary for Open-door Laminoplasty and Titanium Arch Plates for Cervical Myelopathy?

Start date: April 1, 2015
Phase: N/A
Study type: Interventional

This is a randomized controlled trial to assess the use of rigid neck collar postoperatively. It consists of patients with cervical myelopathy undergoing open-door laminoplasty with titanium arch plates. Patients are divided into two groups: one group are not using rigid neck collar whereas the second group of patients wear rigid neck collar for three weeks postoperatively. Both groups of patients will then be assessed at fixed intervals. Clinical assessments include the cervical spine range of motion, any axial neck pain and also a full neurological examination. Radiographs will be used to assess for any complications. Cervical spine alignment and relevant questionnaires will be done and recorded. These results will help to conclude whether we can avoid the use of rigid cervical collars postoperatively, in view of the associated problems arising from restricted neck movement.

NCT ID: NCT03396055 Completed - Clinical trials for Cervical Radiculopathy

Investigation in Integrated Perspective of Radiculomyelopathy Patients

Start date: August 13, 2015
Phase: N/A
Study type: Interventional

Cervical radiculopathy and myelopathy are common degenerative disorders, which can create a large amount of social and medical burden. The aims of this study are(1) to investigate the functional outcomes progression before and after surgery, (2) to evaluate the biomechanical change and compensatory patterns of patients with or without decompression surgery, and (3) to design innovation intervention for the patients with cervical myelopathy and radiculopathy.

NCT ID: NCT03304236 Completed - Cervical Myelopathy Clinical Trials

Motion Analysis of the Myelopathy Hand: New Insight Into the Classical Sign

Start date: July 1, 2017
Phase:
Study type: Observational

This study aims to quantify the clumsiness and decreased dexterity seen in the grip and release test using a simple glove with sensors that can quantify the abnormal motion of this classical sign. This new tool will give a mechanistic insight into the myelopathy. The findings of this study will also form the basis of a prospective longitudinal study with clinical and radiological evaluation to compare the prognosticating value of this new information in clinical practice.

NCT ID: NCT02842775 Completed - Cervical Myelopathy Clinical Trials

Clinical Evaluation and Rehabilitation System for Dynamic Balance Control in Cervical Myelopathy Patients

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

Cervical myelopathy is common among the aging population.One of the complications of cervical myelopathy is balance impairment.In this study, the patients with cervical myelopathy undergo biomechanical, imaging, neurophysiological and functional assessment. Besides, the dynamic balance training is introduced to the patients with cervical decompression surgery.This study is expected to provide important empirical evidence to evaluate the prognosis of the surgery, to further guide the postoperative rehabilitation of myelopathy patients and to improve patients' long-term quality of life.

NCT ID: NCT02758899 Terminated - Diabetes Clinical Trials

Diabetes and Glycosylation in Cervical Spondylosis

Start date: March 2014
Phase:
Study type: Observational

The purpose of this study is to determine the relevant significance of diabetes on cervical disc degeneration, and correlate diabetic control (HgbA1C) with disc glycosylation profile in patients undergoing anterior cervical discectomy and fusion for cervical spondylosis. Additionally, to compare the level of degenerative cervical disc glycosylation in patients with and without diabetes. Hypothesis: Patients with diabetes and degenerative cervical disc disease have higher levels of disc tissue glycosylation, and higher levels of glycosylation are correlated with poor outcomes.

NCT ID: NCT02125981 Completed - Cervical Myelopathy Clinical Trials

The Study About the Efficacy of Oral Limaprost After Surgery for Cervical Myelopathy

Start date: September 1, 2014
Phase: Phase 3
Study type: Interventional

The limaprost alfadex can improve the surgical outcomes in patients with cervical myelopathy.

NCT ID: NCT02068547 Terminated - Radiculopathy Clinical Trials

Bone Marrow Aspirate Concentration in Posterior Cervical Fusion

BMAC
Start date: February 2014
Phase: N/A
Study type: Interventional

The purpose of this research is to test if that combining bone marrow aspirate (removing bone marrow with a needle) concentration with locally harvested (collected) autograft (patient's own bone from another part of the body) for use as the bone graft results in equal rates of a successful procedure (fusion), as compared to current best practice in high-risk patients undergoing posterior cervical fusion. Hypothesis: Bone marrow aspirate concentration combined with locally harvested autograft results in equivalent rates of bony fusion, as compared to current best practice in high-risk patients undergoing posterior cervical decompression and fusion.

NCT ID: NCT01027546 Completed - Cervical Myelopathy Clinical Trials

Effect of Tranexamic Acid on Reducing Postoperative Blood Loss in Cervical Laminoplasty

Start date: January 2007
Phase: N/A
Study type: Interventional

The purpose is to evaluate the efficacy of tranexamic acid in cervical laminoplasty; the surgical procedure used was identical in all cases.