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  • ARC-IM System To Manage Symptomatic Blood Pressure Instability Secondary To Chronic Spinal Cord Injury Rochester, Minn. Empower BP is a pivotal, interventional, multicenter, prospective, randomized, sham-controlled double-blinded study to evaluate the safety and effectiveness of the ARC-IM System in managing symptomatic blood pressure instability in individuals with chronic SCI (\>1 year after SCI).

    The primary effectiveness outcome will be evaluated through subject-reported ADFSCI and seated blood pressure assessments at 3 months post-implant.

    Following a baseline screening period and the surgical implantation of the ARC-IM System, subjects will be randomized with a 2:1 ratio into an active or control arm for 3 months. All the subjects will undergo therapy activation sessions (active or sham) within 21 days of the surgical implant and will then commence independent at-home use of ARC-IM Therapy. At the 3 Month timepoint, after all assessments are conducted, all subjects will transition to the open-label period in order to receive the active version of the ARC-IM System in an open-label fashion. All subjects will undergo therapy programming sessions following Month 3.
  • Characterization Of Transcutaneous Spinal Cord Stimulation Enabling Reflex Motor Evoked Responses In Pediatric Humans With Spina Bifida Rochester, Minn.

    The purpose of this study is to characterize the motor function deficits specific to muscle weakness, intra and interlimb coordination, and the presence, or absence of spasticity.

  • Epidural Spinal Stimulation User Experience Survey for Individuals with Paralysis Due to Spinal Cord Injury Rochester, Minn.

    This is a survey study to identify user-reported motor, sensory, and autonomic functions that are enabled by epidural stimulation, establish correlations between epidural stimulation usage, rehabilitation, functional gains, and user experience in the laboratory and community settings, and to understand and identify subjective goals, benefits, and barriers that still exist with implanted epidural stimulator community.

  • Mayo Clinic Spinal Cord Injury (SCI) Rehabilitation Research Registry Rochester, Minn.

    This will be a prospective registry conducted and maintained at Mayo Clinic Rochester from which collaborating sites within Mayo, Mayo Health Systems, and other spinal cord injury centers can draw from in order to fulfill research enrollment. The information collected for this registry will be used for recruitment purposes only, and will not be used as research data. Participants who are recruited to participate in other research studies will need to complete a separate consenting/enrollment process specific to that study.

     

  • Minnesota Spinal Cord Injury Data Network Rochester, Minn.

    This is a study to generate feasibilty data regarding the collection of health and psychosocial outcomes after acquired spinal cord injury (SCI)

  • Toward Use of the Synergy-based SoftHand Pro for Activities of Daily Living by Persons With Transradial Limb Loss: A Multi-site Clinical Trial Rochester, Minn.

    The purpose of this study is to compare the performance of the SoftHand Pro (SHP) and Ossur i-Limb in grasping and manipulations tasks, and to determine how grasping and manipulation performance improves over time with each device.  Data will also be obtained regarding usage patterns and user satisfaction with each device.

Closed for Enrollment

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