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Spinal Cord Injuries clinical trials

View clinical trials related to Spinal Cord Injuries.

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NCT ID: NCT01297647 Completed - Neurogenic Bladder Clinical Trials

Incidence of Urinary Tract Infection After Urodynamic Investigation

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

The purpose of this study is to evaluate the incidence of urinary tract infection after urodynamic investigation and to identify the involved germs.

NCT ID: NCT01279811 Completed - Spinal Cord Injury Clinical Trials

The Canadian Multicentre CSF Monitoring and Biomarker Study

CAMPER
Start date: January 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to: 1. Measure the pressure in the spinal fluid surrounding the spinal cord to find out how well the spinal cord is being supplied with blood. 2. Determine how drugs called "vasopressors", which are used to control blood pressure following SCI (spinal cord injury), influence spinal fluid pressure. 3. Characterize the severity of an SCI using the levels of specific proteins found within the spinal fluid. 4. Predict how much neurologic recovery may be regained using the levels of specific proteins within your spinal fluid. 5. Identify proteins within the spinal fluid that will help us learn more about what is happening after SCI and assist us in developing new treatments for SCI.

NCT ID: NCT01274975 Completed - Spinal Cord Injury Clinical Trials

Autologous Adipose Derived MSCs Transplantation in Patient With Spinal Cord Injury.

MSC
Start date: July 2009
Phase: Phase 1
Study type: Interventional

This study is designed to assess the safety of intravenous autologous adipose derived mesenchymal stem cells transplant in spinal cord injury patients.

NCT ID: NCT01274312 Completed - Clinical trials for Spinal Cord Injuries

Somato-sensory Reflex Arch in Spinal Cord Injury - Effect on Colorectal Transport

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

Spinal cord injury (SCI) usually affects young people and causes severe bowel and bladder dysfunction. Recently, the concept of a surgically created somato-sensory reflex arch for bladder dysfunction in SCI has been introduced. The concept is promising, not just for bladder but also for bowel dysfunction. However, well designed studies need to be performed before recommending the procedure to a large number of patients worldwide. In this study the investigators perform multidisciplinary studies providing necessary information about the clinical outcome of the somato-sensory reflex arch in adult SCI patients. The hypothesis is as follows: 1. Somato-sensory reflex arch increases colorectal transport between defecations 2. Somato-sensory reflex arch improves colorectal emptying at defecation

NCT ID: NCT01272349 Completed - Spinal Cord Injury Clinical Trials

Intermittent Hypoxia Elicits Prolonged Restoration of Motor Function in Human SCI

Start date: December 2010
Phase: Phase 1
Study type: Interventional

The goal of the study is to determine whether repeatedly breathing low oxygen levels for brief periods (termed intermittent hypoxia) will improve limb function after spinal cord injury. This idea stems from animal studies on respiration, in which investigators have shown that mild intermittent hypoxia improves breathing in spinally injured rats. These studies have shown that intermittent hypoxia induces spinal plasticity, strengthening neural connections and motor neuron function within the spinal cord. Exposure to mild intermittent hypoxia triggers a cascade of events, including increased production of key proteins and increased sensitivity of spinal cord circuitry necessary for improved breathing. The ultimate goal of this research is to assess the potential of mild intermittent hypoxia as a therapeutic approach to stimulate recovery of limb function in human patients.

NCT ID: NCT01272336 Completed - Spinal Cord Injury Clinical Trials

Study Effects of Intermittent Hypoxia on Restoring Hand Function Following SCI

Start date: December 2010
Phase: Phase 1
Study type: Interventional

The goal of the study is to examine the effects of repeated breathing episodes of mild intermittent hypoxia (reduced oxygen) training on hand strength and grasping ability following cervical spinal injury, and to determine whether these changes result in improved hand function. If so, such changes may indicate hypoxia-induced spinal plasticity (ability of the nervous system to strengthen neural pathways based on new experiences), which could result in improvements in hand use for persons with spinal cord injury (SCI).

NCT ID: NCT01272011 Completed - Clinical trials for Spinal Cord Injuries

Effects of Breathing and Walking Treatments on Recovery Post-Spinal Cord Injury

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

The purpose of this study is to determine (1) if a specific breathing treatment (intermittent hypoxia) can promote changes in breathing function and (2) if pairing breathing treatments (hypoxia) with locomotor training can enhance the benefits of walking recovery observed with locomotor training alone (without breathing treatments).

NCT ID: NCT01251549 Completed - Paraplegia Clinical Trials

Safety and Performance Evaluation of ReWalk Reciprocating Gait Orthosis (RGO)

Start date: March 2009
Phase: N/A
Study type: Interventional

ReWalk suit developed by Argo Medical Technologies is designed to enable people with lower limb disabilities to carry out routine ambulatory functions (stand, walk etc.); it can be used by people with disabilities such as spinal cord injury, brain injury, stroke, multiple sclerosis, cerebral palsy and other pathologies that produce severe walking impairments.

NCT ID: NCT01244594 Completed - Spinal Cord Injury Clinical Trials

The Effects of Two Functional Electrical Stimulation Cycling Paradigms

Start date: July 2010
Phase: Phase 2/Phase 3
Study type: Interventional

Background: People with spinal cord injury (SCI) are at risk for many health conditions, some of which can be decreased with exercise. Cycling with Functional Electrical Stimulation (FES) is one way to obtain exercise after SCI. However, cycling with FES has only been done one way, which involves pedaling more quickly with less force to work against. Pedaling more slowly would allow the person to work against more force, which may lead to greater improvements in bone mineral density and muscle size. It may also lead to greater changes in bone make-up, body fat, and cholesterol levels. All of these improvements may lead to a decrease in bone fractures and cardiovascular disease, two major medical issues that exist in the SCI population. Study Aims: This study will compare the outcomes on bone, muscle and cardiovascular health between the commonly used method of pedaling more quickly to a new method of pedaling more slowly. Both groups will work against the maximal force possible. It is expected that the group pedaling more slowly will work against greater force and thus will have improved outcomes compared to other group pedaling faster. Methods: Twenty people with SCI, ages 18-65 years, will be randomly assigned to a treatment group and will participate in three 60-minute sessions per week for 6 months at an outpatient rehabilitation center. All subjects must have complete paralysis of both legs, but may have sensation preserved. Before and after 6 months of exercise, subjects will have an MRI scan to assess muscle size and bone, a dexascan to assess bone, a strength test using electrical stimulation to assess muscle force, an analysis of fat free body tissue, and lab work to measure cholesterol, bone factors that provide insight into bone change, and nutritional status. Relevance: If the protocol of pedaling more slowly results in greater improvements, this technique can be applied to clinical practice. Some people with SCI have FES cycles in their homes and many have been cycling for many years. This new technique may allow them to obtain more benefits than what they currently are receiving from FES cycling. In addition, it is important to maintain overall bone, muscle and cardiovascular health so that people with SCI are health and ready when spinal cord regeneration becomes clinically available.

NCT ID: NCT01241630 Completed - Spinal Cord Injury Clinical Trials

Somato-sensory Reflex Arch in Spinal Cord Injury - Effect on Clinical Outcome

Start date: November 2009
Phase: N/A
Study type: Interventional

Spinal cord injury (SCI) usually affects young people and causes severe bowel and bladder dysfunction. Recently, the concept of a surgically created somat-sensory reflex arch for bladder dysfunction in SCI has been introduced. The concept is promising, not just for bladder but also for bowel dysfunction. However, well designed studies need to be performed before recommending the procedure to a large number of patients worldwide. In this study we perform multidisciplinary studies providing necessary information about the clinical outcome of the somato-sensory reflex arch in adult SCI patients. The hypothesis is as follows: 1. In a "western setting" the somato-sensory reflex arch can be created in adult SCI patients with only minor morbidity and complications. 2. Somato-sensory reflex arch reduces bladder and bowel symptoms in SCI patients.