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Spinal Cord Injury (SCI) clinical trials

View clinical trials related to Spinal Cord Injury (SCI).

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NCT ID: NCT03833674 Completed - Clinical trials for Spinal Cord Injury (SCI)

FLO2 for Recovery After SCI

Start date: August 15, 2020
Phase: N/A
Study type: Interventional

Acute intermittent hypoxia (AIH) involves short (~1-2min) bouts of breathing low oxygen air to stimulate spinal neuroplasticity. Studies in rodents and humans indicate that AIH improves motor function after spinal cord injury (SCI). This study will use a double blind, cross-over design to test if the combination of AIH and respiratory strength training improves breathing function more than either approach alone in adults with chronic SCI.

NCT ID: NCT02469675 Completed - Clinical trials for Amyotrophic Lateral Sclerosis (ALS)

Brain and Nerve Stimulation for Hand Muscles in Spinal Cord Injury and ALS

Start date: June 2015
Phase: N/A
Study type: Interventional

Most neurological injuries such as spinal cord injuries (SCI) and amyotrophic lateral sclerosis (ALS) spare a portion of nerve circuitry. Strengthening spared nerve circuits may be an important method to improve functional recovery. In this study, the investigators aim to use non-invasive magnetic and electrical stimulation to strengthen motor circuits between the brain and hands. Magnetic stimulation will be used over the motor cortex (scalp). Two methods of electrical stimulation will be compared: stimulation of the median nerve at the wrist; or direct stimulation of the cervical spinal cord across the skin on the back of the neck. Several different combinations of magnetic and electrical stimulation will be compared to find the conditions that best strengthen nerve circuits between the brain and hands - "Fire Together, Wire Together". PLEASE NOTE, THIS IS A PRELIMINARY STUDY. This study is testing for temporary changes in nerve transmission and hand function. THERE IS NO EXPECTATION OF LONG-TERM BENEFIT FROM THIS STUDY. If we see temporary changes in this study, then future studies would focus on how to prolong that effect.

NCT ID: NCT02122276 Completed - Clinical trials for Spinal Cord Injury(SCI)

Effects of Continuous Passive Motion on the Spinal Circuitries and Its Adaptation in Patients With Spasticity Resulting From Upper Motor Neuron Lesions

Start date: January 2010
Phase: N/A
Study type: Interventional

In animal and human studies, histochemical and physiological evidences showed that the muscle transferred from slow, fatigue-resistant muscle to fast, fatigable muscle after spinal cord injury. The alternation of muscular property was accompanied by the alternation of spinal circuitry property, and was related to the immobilization adaptation. Previous study showed that remobilization by continuous passive motion (CPM) for one month would restore the function of spinal circuitry in individual with chronic SCI. It is possible that long term application of CPM can reverse the adaptation of contractile properties of the paralyzed muscle after SCI. The purpose of this study is to investigate the effect of a four month CPM training on muscular properties in individuals with chronic SCI.

NCT ID: NCT02052024 Completed - Stroke Clinical Trials

Myobloc Atrophy Study

MAS
Start date: May 2014
Phase: Phase 4
Study type: Interventional

The present pilot study is designed to assess the extent to which BOTOX and MYOBLOC cause muscle atrophy in spastic patients. The primary objective is to assess whether there is statistically significant difference in muscle atrophy between the two groups over a one year period.

NCT ID: NCT01988142 Completed - Clinical trials for Spinal Cord Injury(SCI)

The Effect of Continuous Passive Motion Training on Neuromuscular Adaptation

Start date: August 2006
Phase: N/A
Study type: Interventional

After spinal cord injury (SCI), the muscular property altered due to the immobilization adaptation. The purpose of this study was to investigate the effect of remobilization with continuous passive exercise on the adapted paralyzed muscle properties after SCI.

NCT ID: NCT01232907 Completed - Clinical trials for Spinal Cord Injury (SCI)

The Effects of L-carnitine on Fatigue in Spinal Cord Injury

Start date: October 2010
Phase: Phase 2
Study type: Interventional

1. Purpose: To explore the use of L-Carnitine, a pharmaceutical product, for the treatment of fatigue in persons with spinal cord injury (SCI). 2. Hypothesis: Similar to previous research in disabled and aging populations, the investigators hypothesize that treatment with L-Carnitine will result in a significant improvement of clinical fatigue in spinal cord injury clients, effecting a decrease on the Fatigue Severity Scale (FSS) of 0.5 points or more. The investigators expect to see an effect after approximately three weeks of treatment. As secondary outcomes, the investigators expect to see positive changes in the Centre for Epidemiologic Studies Depression Scale (CES-D)and Visual Analogue Fatigue (VAS-F) and Visual Analogue Pain (VAS-P) scores, due to a combination of previously demonstrated effects of L-Carnitine directly on pain and depression, and the effects of the potential decrease in fatigue.

NCT ID: NCT00488280 Completed - Clinical trials for Spinal Cord Injury (SCI)

Restoring Walking in Non-ambulatory Children With Severe Chronic Spinal Cord Injury (SCI) (Kids STEP Study)

Start date: February 2007
Phase: Phase 1
Study type: Interventional

The Kids STEP Study aims to 1. Determine if walking can be restored in children with incomplete SCI and little to no leg movement 2. Identify the neural pathways that permit recovery of walking