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Spinal Cord Injuries clinical trials

View clinical trials related to Spinal Cord Injuries.

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NCT ID: NCT01204047 Completed - Spinal Cord Injury Clinical Trials

Wheelchair Mobility Assessment of Individuals With Spinal Cord Injury

Start date: March 2008
Phase: N/A
Study type: Observational

The specific aims of this study are: 1) to assess the test-retest reliability of a modification of an existing wheelchair propulsion assessment and 2) validate the modification against traditional measures of physical strength, power, and endurance in a group of persons with spinal cord injury (SCI).

NCT ID: NCT01203150 Completed - Spinal Cord Injury Clinical Trials

Effects of Exercise in People With Paraplegia

Start date: October 2008
Phase: N/A
Study type: Interventional

This hypothesis-driven study will investigate effects of physical activity with or without a nutrient supplement known to increase body lean mass in adults with chronic paraplegia who have clusters of obesity and obesity-related secondary complications.

NCT ID: NCT01202227 Completed - Pain Clinical Trials

An Open-Label Long-Term Study Of Pregabalin For The Treatment Of Central Neuropathic Pain

Start date: September 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the safety of the long-term use of pregabalin at doses up to 600 mg/day in patients with central neuropathic pain (post spinal cord injury pain, post stroke pain, and multiple sclerosis pain).

NCT ID: NCT01202019 Completed - Spinal Cord Injury Clinical Trials

Effects of Exercise in People With Tetraplegia

Start date: March 2008
Phase: N/A
Study type: Interventional

This study is designed to assess the impact of exercise and supplementation on measures of fitness, function, and cardiovascular disease risk factors/modifiers in individuals with spinal cord injury (SCI). The primary purpose of this study is to improve fitness and function, reduce cardiovascular disease risks, and enhance oxidation of dietary and body fats in persons with chronic tetraplegia through acute exercise, exercise conditioning, and dietary supplementation. This study will test the hypothesis that timing of supplementation with regards to exercise bout ('intervention/placebo') affects fitness, function, lipid profiles, lipid oxidation, and inflammatory markers after acute exercise and chronic conditioning.

NCT ID: NCT01201759 Completed - Spinal Cord Injury Clinical Trials

Effects of Salsalate on Prandial-Induced Vascular Inflammation After Spinal Cord Injury (SCI)

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

The overall study objectives are to examine whether: 1. Persons with spinal cord injury (SCI) having elevated body mass are at greater cardiovascular disease (CVD) risk for fasting and postprandial lipidemia, glycemia, and vascular inflammation than persons with SCI having 'normal' body mass, and 2. An inexpensive, low-risk, widely-available pharmacotherapy safely reduces CVD risks associated with fasting and postprandial lipidemia, glycemia, and vascular inflammation.

NCT ID: NCT01197599 Completed - Spinal Cord Injury Clinical Trials

Acute Tendon and Nerve Responses to Exercise

Start date: December 2008
Phase: N/A
Study type: Observational

The purpose of this study is to use ultrasound to analyze the effects of a bout of circuit training on the upper extremity of persons with spinal cord injury and able-bodied controls.

NCT ID: NCT01186679 Completed - Clinical trials for Spinal Cord Injuries

Safety and Efficacy of Autologous Bone Marrow Stem Cells in Treating Spinal Cord Injury

ABMST-SCI
Start date: January 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The projected data related to the burden of spinal cord injuries induced limb paralysis in India is quite alarming. This is attributed to the rapid industrialization and economical development in the country. Increase in vehicular traffic has caused numerous road traffic accidents. Rapid increase in populations, development in the computer technology and real estate business lead to construction of huge buildings which indirectly adds to the injuries due to fall. Spinal cord injuries could not be treated adequately with the prevailing treatment modalities. In view of this, there is definitely an urgent need for finding different methods of treatment for these patients who cannot undergo established modalities of treatment or these have been tried unsuccessfully. Since a large number of these patients will loose their productive life and at the prime of their lives, one such alternate therapy, which seems to offer some promise, is "stem cell" therapy, which has been well studied and published in prestigious journals. In our present study, we want to evaluate the safety and efficacy of autologous bone marrow derived stem cells surgically transplanted directly into the lesion site with glial scar resection for 8 indian patients of chronic spinal cord injury and intra-thecal injection for 4 indian patients of acute and subacute injury.

NCT ID: NCT01184742 Completed - Spinal Cord Injury Clinical Trials

6 Minute Push & 30 Second Sprint Tests Reliability & Relationship to Fitness, Participation, & Environmental Assessments

Start date: March 2010
Phase: N/A
Study type: Observational

The purpose of this study is to assess the relationship between physical fitness and wheelchair mobility capacity and 1) participation; 2) self-reported environments barriers; and 3) self-reported avoidance of environmental features.

NCT ID: NCT01184729 Completed - Spinal Cord Injury Clinical Trials

6 Minute Propulsion Test Sensitivity to Increased Aerobic Capacity

Start date: November 2008
Phase: N/A
Study type: Observational

The goals of this project are to 1)determine the responsiveness of the 6 Minute Push Test (6MPT) and 2) explore the relationship between 6MPT distance and measures of handicap, wheelchair satisfaction, depression, and self-reported avoidance of environmental features.

NCT ID: NCT01184365 Completed - Spinal Cord Injury Clinical Trials

Spinal Cord Injury Energy Management Program

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

Fatigue is a common complaint of persons with spinal cord injury (SCI) that negatively affects physical function, participation in daily activities, employment, and community involvement. No behavioural intervention for fatigue has been reported for SCI, though the benefits of such programs have been proven in persons with neurological conditions like multiple sclerosis and arthritis. Based on a study with people with SCI, an energy management program (EnMP-1) was developed. The focus of this study is to test EnMP-1. Adults with SCI living in the community and reporting fatigue as a problem will participate in the program. Hypothesis: Participants in the EnMP-1 group will show significantly lower fatigue impact scores and higher self-efficacy scores immediately after, 3 months, and 6 months post-intervention than EnMP-2 participants.