Status | Study |
Terminated |
Study Name: Evaluation of a Hybrid Prototype Strategy (Electrostimulation of Lower Limb Muscles Associated With Voluntary Strengthening of the Upper Limbs) in Reconditioning to Effort in Patients With Chronic Paraplegia. Condition: Chronic Paraplegia Date: 2014-01-17 Interventions: Other: strengthening Other: hybrid trainin |
Completed |
Study Name: Safety of Autologous Human Schwann Cells (ahSC) in Subjects With Subacute SCI Condition: Spinal Cord Injury Paraplegia Date: 2012-11-28 Interventions: Biological: Autologous Human Schwann Cells Schwann cells harvested from the sural nerve of the participa |
Withdrawn |
Study Name: Study of the Impact of the Use of a Corset on the Respiratory Function of Patients With Spinal Cord Injury Condition: Spinal Cord Injury Tetraplegia Parap Date: 2012-03-26 Interventions: Device: Corset the patients are assigned the use of a custome made corset during daytime |
Completed |
Study Name: Use of Interactive Gaming for Enhanced Function After Spinal Cord Injury Condition: Paraplegia and Tetraplegia Date: 2012-02-17 Interventions: Other: Video gaming for enhanced function after spinal cord injury. Spinal cord injured indviduals will |
Terminated |
Study Name: The ReWalk Exoskeletal Walking System for Persons With Paraplegia Condition: Paraplegia Date: 2011-09-14 |
Completed |
Study Name: Safety and Performance Evaluation of ReWalk Reciprocating Gait Orthosis (RGO) Condition: Paraplegia Spinal Cord Injuries (SCI) Date: 2010-11-28 Interventions: Device: ReWalk - a motorized exoskeleton suit The subject will wear the ReWalk suit and have training se |
Completed |
Study Name: Brain Function and White Matter Changes in Congenital, Acute and Chronic Spinal Cord Lesions Condition: Paraplegia, Spinal Myelomeningocele Date: 2010-09-23 Interventions: Other: fMRI, DTI functional magnetic resonance imaging (fMRI), MR diffusion tensor imaging (DTI) |
Completed |
Study Name: Effects of Exercise in People With Paraplegia Condition: Spinal Cord Injury Date: 2010-09-15 Interventions: Other: Exercise CRT will occur 3 times per week for 26 weeks. Each training session will last approximat |
Completed |
Study Name: Efficacy of Nebido on Bone Mineral Density (BMD) in Hypogonadal Paraplegic Patients With Confirmed Osteoporosis Condition: Hypogonadism Paraplegia Bone Date: 2009-02-04 Interventions: Drug: Testosterone Undeconate (Nebido-R, BAY86-5037) Male patients > 18yrs in medical practices fulfi |
Completed |
Study Name: Adjusting Wheelchair Set-Up to Minimize Shoulder Joint Forces During Propulsion Condition: Paraplegia Upper Limb Pain Date: 2008-11-04 |