Clinical Trials Logo

Spinal Cord Injury clinical trials

View clinical trials related to Spinal Cord Injury.

Filter by:

NCT ID: NCT01328860 Terminated - Spinal Cord Injury Clinical Trials

Autologous Stem Cells for Spinal Cord Injury (SCI) in Children

Start date: April 2011
Phase: Phase 1
Study type: Interventional

The purpose of this research study is: 1. To see if Bone Marrow Cell harvest and transplantation are safe in children with Spinal Cord Injury, and 2. To determine if late functional outcome is improved following Bone Marrow Cell transplantation in children with Spinal Cord Injury, using pre-transplantation spinal cord function as the control.

NCT ID: NCT01325103 Completed - Spinal Cord Injury Clinical Trials

Autologous Bone Marrow Stem Cell Transplantation in Patients With Spinal Cord Injury

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

This research investigates the use of autologous bone marrow stem cells in patients with spinal cord injury.

NCT ID: NCT01321333 Completed - Spinal Cord Injury Clinical Trials

Study of Human Central Nervous System Stem Cells (HuCNS-SC) in Patients With Thoracic Spinal Cord Injury

Start date: March 2011
Phase: Phase 1/Phase 2
Study type: Interventional

This study will evaluate the effect of single transplantation of HuCNS-SC cells into the thoracic spinal cord of patients with sub-acute spinal cord injury.

NCT ID: NCT01299792 Completed - Spinal Cord Injury Clinical Trials

Sonographic Measurement of Bladder Wall Thickness in Patients With Neurogenic Bladder Dysfunction

Start date: August 2009
Phase:
Study type: Observational

Video-urodynamic investigations are regarded as the current standard diagnostics for neurogenic bladder dysfunction in patients with spinal cord injury. This examination is exact, but time consuming, costly and associated with the risk of urinary tract infection. In patients with lower urinary tract symptoms due to benign prostate hyperplasia, sonographic measurement of bladder wall thickness has been demonstrated to be able to replace urodynamic testing for the diagnosis of infravesical obstruction. Hypothesis: measurement of bladder wall thickness in patients with neurogenic bladder dysfunction due to spinal cord injury is closely related to the known risk factors for upper urinary tract deterioration (bladder compliance, detrusor leak point pressure) in this group of patients and can therefore replace urodynamic examination in selected cases.

NCT ID: NCT01297673 Completed - Spinal Cord Injury Clinical Trials

Reflux in Spinal Cord Injury Patients With Neurogenic Lower Urinary Tract Dysfunction

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

The purpose of this study is to investigate the incidence of reflux in patients with spinal cord injury in relation to the lesion level, duration of injury and bladder management

NCT ID: NCT01292941 Withdrawn - Spinal Cord Injury Clinical Trials

Clinical Study Evaluating Safety of a New Catheter for Urinary Intermittent Catheter in Healthy Volunteers

Start date: March 2011
Phase: Phase 1
Study type: Interventional

To evaluate discomfort of a new coating and catheter material compared to SpeediCath (SC)

NCT ID: NCT01292811 Terminated - Spinal Cord Injury Clinical Trials

Restoration of Upper Limb Function in Individuals With Sub-Acute Spinal Cord Injury

MCRCT
Start date: January 2011
Phase: N/A
Study type: Interventional

The objective of this research program is to conduct a multi-site clinical randomized control trial that will evaluate the efficacy of functional electrical stimulation based upper limb intervention for people with tetraplegia. This will involve recruiting 84 persons with sub-acute tetraplegia across four sites (Montreal,Toronto, Fredericton and Edmonton) and will serve to evaluate three new Canadian hand function assessments that have been specifically developed for persons with tetraplegia. Although these assessments have been recently tested and have shown considerable promise, further evaluation on their clinical utility (in particular their responsiveness and validity) is required. As well, they need to be compared with one another to determine whether any of these tests is more appropriate for clinical applications or whether further test reduction or augmentation may be required. Having measures that are sensitive and accurate in assessing hand function is key for systematically evaluating emerging therapeutic interventions.

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: 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.