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Spinal Cord Injury clinical trials

View clinical trials related to Spinal Cord Injury.

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NCT ID: NCT00291317 Completed - Spinal Cord Injury Clinical Trials

The Effect of FES on Children With Spinal Cord Injury

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

Regular exercise is strongly recommended to help maintain a healthy lifestyle. Unfortunately, children and young adults with damaged spinal cords may not be able to exercise regularly. However, there is an exercise bike specially designed for persons with damaged spinal cords that enables them to pedal by directly stimulating the muscles in their legs. Our study is designed to determine the benefits of exercise for Spinal Cord Injured (SCI) patients using this bike.

NCT ID: NCT00286520 Completed - Spinal Cord Injury Clinical Trials

Treatment of Fecal Incontinence and Constipation in Patients With Spinal Cord Injury

Start date: December 2003
Phase: Phase 4
Study type: Interventional

The study aims to compare a newly developed system for transanal colonic irrigation (Peristeen Anal Irrigation) with a bowel management regime that does not include irrigation in a prospective, randomized trial in spinal cord lesion patients (SCL- patients) with faecal incontinence and/or constipation. Population; 80 SCL- patients with faecal incontinence and/or constipation from five countries. Focus on: Bowel symptom score Neurogenic Bowel Dysfunction score Symptom related quality of life questionnaire Time expenditure for performance of bowel care ans side effects

NCT ID: NCT00270855 Completed - Obesity Clinical Trials

Exercise to Reduce Obesity in Spinal Cord Injury

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

The purpose of this proposal was to evaluate and compare the health benefits of using upper extremity exercise versus functional electrical stimulation for lower extremity exercise. It was our hypothesis that both Functional Electrical Stimulation Leg Cycle Ergometry (FES LCE) exercise and voluntary Arm Crank Ergometry (ACE) upper extremity exercise would increase whole body energy expenditure, thereby increasing muscle mass, insulin sensitivity, glucose effectiveness and improving lipid profiles in adults with paraplegia.

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: NCT00262457 Withdrawn - Spinal Cord Injury Clinical Trials

BIONs, for Improved Tissue Health and Pressure Sore Prevention

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

The purpose of this study was to determine the feasibility of an implanted electrical stimulation system incorporating BION microstimulators for long term use to prevent tissue breakdown in high risk patients.

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: NCT00228085 Not yet recruiting - Spinal Cord Injury Clinical Trials

Changes of Parameters of Transcranial Magnetic Stimulation in Patients With Spinal Cord Injury

Start date: September 2005
Phase: N/A
Study type: Observational

CNS reorganization is evidenced in patients with CNS lesion, no exception to the patients with spinal cord injury. The paraplegics have to increase their loading of upper extremities to compesate the lost function of lower extremities. We hypothesize that CNS reorganization can happen in the chronic paraplegics. We try to compare the changes of parameters of transcranial magnetic stimulation in these patients with the normal population cross-sectionally.

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.