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Spinal Cord Diseases clinical trials

View clinical trials related to Spinal Cord Diseases.

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NCT ID: NCT06188130 Active, not recruiting - Clinical trials for Chronic Spinal Cord Disorder

The Effects of rTMS and tDCS Combined With Robotic Rehabilitation In Patients With Spinal Cord Injury

Start date: January 15, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the effect of rTMS and tDCS combined with robotic therapy on motor functional recovery and gait parameters

NCT ID: NCT05696470 Active, not recruiting - Radiculopathy Clinical Trials

Fusion Rates of 3D Printed Porous Titanium Cages in Three and Four Level ACDFs

Start date: March 31, 2021
Phase:
Study type: Observational [Patient Registry]

The purpose of this trial is to assess fusion rates in 3 and 4 level ACDFs in patients implanted with DePuy Conduit 3D printed titanium cages supplemented with SKYLINE Anterior Cervical Plate System and 1 CC DBM. This will be a non-inferiority study, looking to show that Synthes Conduit 3D printed titanium cages fuse as well as cages.

NCT ID: NCT05669508 Active, not recruiting - Clinical trials for Spinal Cord Injuries

Wearable Electrical Stimulation on the Back to Modulate Spinal Cord Activity

RISES-T
Start date: February 10, 2022
Phase: N/A
Study type: Interventional

The goal of this study is to evaluate if non-invasive electrical spinal stimulation can help people with paralysis caused by SCI improve strength and function of their arms, legs, hands or feet. The study will involve therapy sessions involving exercises done at the same time as electrical stimulation therapy. This study has multiple parts to evaluate the effectiveness and safety of "smart" electrical stimulation of the spinal cord, which involves stimulating the spinal cord at precise locations and times to improve movement and function.

NCT ID: NCT04955041 Active, not recruiting - Clinical trials for Cervical Spondylotic Myelopathy

Effectiveness of T2* MRI in Cervical Spondylotic Myelopathy

Start date: January 2010
Phase:
Study type: Observational

Utilization of T2* MRI in predicting prognosis in patients with cervical spondylotic myelopathy (CSM)

NCT ID: NCT03534518 Active, not recruiting - Clinical trials for Spinal Cord Diseases

Body Weight Supported Training Study

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

Successful ambulation at home and in the community is the main goal of gait training after incomplete spinal cord injury. Many different treatment approaches have been recommended to achieve this goal. One established intervention to achieve that in a clinical setting is body weight supported (BWS) treadmill training. However, recent studies have suggested that the most optimal gait training should be conducted overground with appropriate support conditions to enable a physiological gait pattern. The training has to be challenging and patients must participate as active as possible. In addition becoming a functional walker in real world involves a variety of walking skills like walking on uneven surfaces, walking up and down slopes, climbing stairs and avoid obstacles. It has been shown in humans as well as in animals that greater improvements are achieved in walking function if the training is task specific. Thus a constrained task like BWS treadmill training may not be the optimal training intervention to become a functional community walker. Even greater improvements can be expected if patients feel safe during the overground walking and train at their individual limits. With FLOAT there is now the possibility to conduct a task specific BWS overground gait training in a safe environment. The robotic device allows patients to perform different walking tasks like walking overground, avoiding obstacles, walking on uneven and sloped surfaces, climbing stairs, walking in narrow spaces. A virtual reality setup was integrated into the system that even can simulate specific walking tasks like target oriented walking or walking in crowded environment. Based on the promising results seen in preclinical and clinical research, the investigators assume that unrestricted transparent BWS overground training that allows task specific training of real world walking tasks will induce greater improvements than conventional BWS treadmill training. The investigators will compare the effect of an intensive 4 weeks unrestricted BWS overground gait training to 4 weeks of intensive BWS treadmill training. Not only functional outcome like walking speed or capacity will be assessed but also detailed kinematics that will help to identify the mechanisms of the underlying improvements in walking function.

NCT ID: NCT03503513 Active, not recruiting - Clinical trials for Spinal Cord Injuries

Gentamicin Bladder Instillations to Prevent Urinary Tract Infections in Patients With Spinal Cord Injury

Start date: August 24, 2018
Phase: Phase 2/Phase 3
Study type: Interventional

A non-randomized study evaluating the efficacy of intravesical gentamicin on the occurrence rate of urinary tract infections and bladder complications in patients after spinal cord injury (SCI), and to assess its effectiveness in promoting overall quality of life (QOL), community living, and participation.

NCT ID: NCT03296592 Active, not recruiting - Clinical trials for Cervical Spondylotic Myelopathy

Diffusion MRI in Cervical Spondylotic Myelopathy (CSM)

CSM
Start date: January 29, 2018
Phase:
Study type: Observational

Patients who have been diagnosed with Cervical Spondylotic Myelopathy will be asked to undergo an MRI using diffusion basis spectrum imaging (DBSI) technology. The patients will have this MRI preoperatively and at 24 months postop. The investigators believe that with this imaging, biomarkers will be able to be seen to assist in prediction of long term outcomes in patients with spinal cord compression. These patients will be compared to healthy cohorts who will also undergo an MRI using the DBSI technology.

NCT ID: NCT02076113 Active, not recruiting - Clinical trials for Cervical Spondylosis With Myelopathy

Cervical Spondylotic Myelopathy Surgical Trial

Start date: April 1, 2014
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the optimal surgical approach (ventral vs dorsal) for patients with multi-level cervical spondylotic myelopathy (CSM). There are no established guidelines for the management of patients with CSM, which represents the most common cause of spinal cord injury and dysfunction in the US and in the world. This study aims to test the hypothesis that ventral surgery is associated with superior Short Form-36 physical component Score (SF-36 PCS) outcome at one year follow-up compared to dorsal approaches and that both ventral and dorsal surgery improve symptoms of spinal cord dysfunction measured using the modified Japanese Orthopedic Association Score (mJOA). A secondary hypothesis is that health resource utilization for ventral surgery, dorsal fusion, and laminoplasty surgery are different. A third hypothesis is that cervical sagittal balance post-operatively is a significant predictor of SF-36 PCS outcome.

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.