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Spinal Cord Injuries clinical trials

View clinical trials related to Spinal Cord Injuries.

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NCT ID: NCT00266864 Completed - Spinal Cord Injury Clinical Trials

Testosterone Replacement Therapy in Chronic Spinal Cord Injury

Start date: August 2003
Phase: Phase 2/Phase 3
Study type: Interventional

It has long been recognized that co-morbidity associated with multiple metabolic syndrome, such as adverse body composition, insulin resistance and autonomic nervous system impairment, may lead to significant increase in cardiovascular morbidity and mortality. It is unclear whether the co-morbidity evident in this population are due directly to their immobility or are the result of unfavorable changes in their underlying hormonal milieu. The purpose of this study is to determine the effect of testosterone replacement therapy in hypogonadal males on: body composition, i.e. lean tissue and fat mass, glucose tolerance, resting energy expenditure, autonomic-cardiovascular integrity, muscular strength, psychological assessment

NCT ID: NCT00252954 Completed - Pain Clinical Trials

Levetiracetam in Chronic Neuropathic Pain Following Spinal Cord Injury

Start date: November 2005
Phase: Phase 4
Study type: Interventional

Purpose: To evaluate the efficacy and safety of levetiracetam on chronic neuropathic pain after spinal cord injury, and to examine its effect on spasms and evoked pain.

NCT ID: NCT00248807 Completed - Clinical trials for Spinal Cord Injuries

A Study of Blood Pressure and Blood Supply to the Brain in Persons With a Spinal Cord Injury.

Start date: October 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to determine how blood pressure and blood flow are controlled during head-up tilt in a semi-upright position. In this investigation we are studying blood pressure and blood flow to the brain, with and without a medication which lowers blood pressure (Vasotec). We will determine how persons with a spinal cord injury are able to maintain blood flow to the brain (not get dizzy) as they assume a more upright position and their blood pressure decreases.

NCT ID: NCT00245726 Completed - Spinal Cord Injury Clinical Trials

Functional Electrical Stimulation (FES) Cycling for Children With Spinal Cord Injuries (SCI)

Start date: March 2004
Phase: N/A
Study type: Interventional

The overall objective of this research project is to examine the clinical efficacy of lower extremity cycling with functional electrical stimulation to improve the health and fitness of children with spinal cord injuries (SCI). To achieve this goal, a controlled, randomized study will be conducted with thirty children who have sustained a spinal cord injury. The children in the study will be assigned to one of three groups: those receiving functional electrical stimulation (FES) leg cycling exercise, those receiving passive leg cycling, and a non-cycling control group receiving electrical stimulation therapy to generate muscle contractions in the lower extremity. All three groups will be balanced as to the amount of time they receive the specific therapy. All therapies, after initial assessment, will be conducted at home in order to foster changes in lifestyle that may prove to be essential for improved quality of life. The specific aims of this proposal are delineated below: Aim 1: To assess, by means of a randomized controlled study design, the ability of FES cycling to improve the cardiovascular and musculoskeletal systems of ten children with a spinal cord injury, as compared to ten children undergoing passive leg cycling exercise and ten children receiving electrical stimulation therapy alone. Aim 2: To determine, by means of a randomized controlled study design, the feasibility of using FES leg cycling exercise to provide long-term health benefits and improve the neurologic status of ten children with a spinal cord injury, as compared to ten children undergoing passive leg cycling exercise and ten children receiving electrical stimulation therapy alone.

NCT ID: NCT00237770 Completed - Spinal Cord Injury Clinical Trials

Prevention of Low Blood Pressure in Persons With Tetraplegia

Start date: June 2003
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this investigation is to determine the blood pressure response to NOS inhibition, with L-NAME, in persons with tetraplegia compared to non-SCI control subjects and to establish if blood pressure can be increased while upright in those with tetraplegia. If blood pressure is increased with NOS inhibition in persons with tetraplegia, this would improve our treatment of the condition of low blood pressure during seated postures in individuals with tetraplegia.

NCT ID: NCT00223912 Completed - Clinical trials for Cardiovascular Disease

Effect of Exercise on Blood Coagulation in Persons With Chronic Spinal Cord Injury

FES
Start date: November 2003
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if exercise affects the clotting of blood (hemostasis). The effect of exercise on hemostasis will be determined in persons with spinal cord injury, a population reported to have an increased prevalence of cardiovascular disease (CVD). It is expected that this study will increase our understanding of CVD in persons with SCI, and it will eventually help reduce the occurrence of premature heart disease.

NCT ID: NCT00223873 Completed - Spinal Cord Injury Clinical Trials

The Use of Penile Vibratory Stimulation to Decrease Spasticity Following Spinal Cord Injury

Start date: November 2002
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect of penile vibratory stimulation on the muscle spasticity of men with chronic spinal cord injury.

NCT ID: NCT00223860 Completed - Spinal Cord Injury Clinical Trials

Provocative Testing Using LHRH and hCG of the Pituitary-Gonadal Axis in Persons With Spinal Cord Injury.

Start date: July 2001
Phase: N/A
Study type: Interventional

There is evidence that has shown that serum testosterone levels are low in persons with chronic spinal cord injury (SCI). The question arises as to whether the defect in testosterone production is from the hypothalamic pituitary system (part of the brain that plays a role in testosterone release) or from the male testes. Studies to date are inconclusive. This study, will examine if persons with SCI has a normal hormonal regulation of the male hormone testosterone in comparison to persons who are able-bodied. This will help understand the physical and metabolic changes that occur in persons with SCI.

NCT ID: NCT00223769 Completed - Spinal Cord Injury Clinical Trials

The Use of Anabolic Steroids to Improve Function After Spinal Cord Injury

Start date: January 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect of oxandrolone on the function and quality of life of patients with chronic spinal cord injury.

NCT ID: NCT00221767 Completed - Clinical trials for Spinal Cord Injuries

Medico-economical Impact of the Brindley Neurosurgical Technique in France

BRINDLEY
Start date: June 2005
Phase: N/A
Study type: Interventional

Bladder dysfunction is a major problem in patients with complete spinal cord lesions. For patients presenting incontinence or risk for kidney, two major conventional alternatives are possible : conservative therapies (muscarinic receptor antagonists, vanilloids drugs and botulinum toxin in association with catheterization) and surgical techniques intervening in the nervous and urinary system. Among these last alternatives, the Brindley technique (anterior sacral root stimulation with posterior rhizotomy) is the only technique allowing for the restauration of bladder function, continence, and micturition. The purpose of the study is to compare the Brindley technique with the first conventional approach in France from a medical and economical point of view.