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Wounds and Injuries clinical trials

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NCT ID: NCT00320281 Completed - Pain Clinical Trials

Investigating Botulinum Toxin A to Treat Acute Neck/Upper Shoulder Pain Following a New Spinal Cord Injury.

Start date: April 2006
Phase: Phase 4
Study type: Interventional

As clinicians, it is often a struggle to find effective pain control for a certain subgroup of patients with tetraplegia. These patients often have severe upper back, neck, and shoulder pain, limiting rehabilitation productivity and potential, and always limiting quality of life. This pain appears to be primarily musculoskeletal. Muscles in the upper back and neck become shortened, rock hard, and extremely tender with even the slightest touch or stretch. Refractory to multiple classes of medications, modalities, and other treatments, patients truly suffer-not only from pain, but from fatigue, sedation, expense, and loss of useful rehabilitation time due to attempted remedies. Unfortunately, this subgroup of patients is not small and the problem is significant, as anyone who specializes in the treatment of spinal cord injury patients will recognize. In search for another form of treatment, botulinum toxin A (BTXA) may be promising for pain control in that group of patients with tetraplegia whose pain has proven to be refractory to treatment. It did not take long searching the literature to find compelling evidence that BTXA may have another mechanism of action for direct pain control, apart from its well known mechanism for spasticity control. Clinically, it is increasingly being recommended and used for this purpose. In fact, one of the specific indications now recognized by most for BTXA treatment is for myogenic pain due to short, tight, strained muscles-just as we see with our population. Yet, it's application has not been studied in people with tetraplegia. Thus, the genesis of the project and the hope to help our patients evolved. Study hypotheses: - In addition to traditional treatments used for pain control, injection of BTXA into cervical and upper back muscles will effectively reduce cervical/shoulder pain severity reported by individuals with cervical spinal cord injuries, regardless of the etiology of pain. - Pain reduction secondary to the use of BTXA will be associated with a decrease in total analgesic medication use among SCI patients during acute inpatient rehabilitation. - BTXA to treat cervical/shoulder pain will increase active participation in the rehabilitation program for individuals with tetraplegia during inpatient rehabilitation.

NCT ID: NCT00310999 Completed - Wounds and Injuries Clinical Trials

C-Spine Movement - Shikani Optical Scope vs Macintosh Laryngoscope for Patients With Cervical Spine Injury

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

Patients undergoing surgery will have laryngoscopy performed using two widely accepted techniques - Macintosh Laryngoscope and Shikani Optical Scope. The techniques will be timed and compared for cervical spine movement using fluoroscopy.

NCT ID: NCT00285961 Completed - Wounds and Injuries Clinical Trials

Evaluation of Cork Splint Materials Instead of Plaster Splint for Children

Start date: n/a
Phase: N/A
Study type: Interventional

This is an evaluation of the functionality and added value of cork splint materials instead of a plaster splint for children (3-11 years old).

NCT ID: NCT00270959 Completed - Clinical trials for Post-Traumatic Stress Disorder

Patient-Centered Collaborative Care for Preventing Post-Traumatic Stress Disorder After Traumatic Injury

TSOS II
Start date: June 2006
Phase: Phase 1
Study type: Interventional

This study will evaluate the effectiveness of patient-centered collaborative care that combines behavioral therapy and drug therapy as compared to usual care in reducing symptoms of post-traumatic stress disorder in people who have survived a traumatic injury.

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: NCT00266929 Completed - Spinal Injuries Clinical Trials

Treatment of Type II Odontoid Fractures Among the Elderly

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

The purpose of this study is to compare the safety and effectiveness of surgical versus conservative management of type II odontoid fractures among patients > 64 years of age. Of secondary interest is to determine if there are differences in outcomes between anterior screw fixation and posterior fusion of these fractures.

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: NCT00264511 Completed - Tibial Fracture Clinical Trials

Hyperbaric Oxygen in Lower Leg Trauma

Start date: February 13, 2007
Phase: Phase 2/Phase 3
Study type: Interventional

Study hypothesis :Hyperbaric Oxygen may prevent complications and improve outcomes in severe lower limb trauma. We propose to investigate this hypothesis by conducting an International multi centre randomised control trial of standard trauma/orthopaedic care with or without a concurrent course of hyperbaric oxygen treatments.

NCT ID: NCT00263432 Completed - Clinical trials for Cartilage Injuries in the Human Knee

Reparation of Cartilage Injuries in the Human Knee by Implantation of Fresh Human Allogenic Chondrocytes

Start date: August 1, 2011
Phase: N/A
Study type: Interventional

Implantation of fresh human allogenic chondrocytes in human knee cartilage injuries to obtain a repair and prevention of secondary osteoarthritis

NCT ID: NCT00254722 Completed - Clinical trials for Traumatic Brain Injury

Safety of Autologous Stem Cell Treatment for Traumatic Brain Injury in Children

Start date: April 2006
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine if bone marrow progenitor cell (BMPC) autologous transplantation in children after isolated traumatic brain injury is safe and will improve functional outcome.