Cleveland, OHNCT06965127Now EnrollingIRB Ready

Spinal Cord Injury (SCI) Clinical Trial in Cleveland, OH

Access cutting-edge spinal cord injury (sci) treatment through this clinical trial at a research site in Cleveland. Study-provided care at no cost to qualified participants.

Sponsored by Louis Stokes VA Medical Center

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Expert Care in Cleveland

Access spinal cord injury (sci) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related spinal cord injury (sci) treatment provided free

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Check if you qualify for this spinal cord injury (sci) clinical trial in Cleveland, OH

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Cleveland

    Convenient for OH residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Cleveland site if eligible
  4. 4Begin participation

About This Spinal Cord Injury (SCI) Study in Cleveland

This is a device study that will evaluate the effect of an implanted stimulator on improving walking in people with incomplete spinal cord injury. There are two phases in the study: 1) Screening - this phase determines if the individual is a good candidate to receive an implanted system, 2) Implantation, controller development, and evaluation - this phase includes implanting the device and setting the individual up for system use, creating controllers for walking, and evaluating the effect of the device over a couple years.

Sponsor: Louis Stokes VA Medical Center

Who Can Participate

Inclusion Criteria

Between the ages of 18-75
Non-ventilator dependent paralysis resulting from injuries such as: cervical/thoracic spinal cord injuries affecting the trunk and/or lower limbs
Impairment classification of AIS B, C, or D (preservation of sensation and/or some motor function) with weakness in trunk and/or lower extremity muscles
Unable to walk faster than 0.8m/s during a 10m walk test
Gait deviation such as reduced peak hip, knee, and/or ankle range of motion during stance or swing phases due to motor impairment
Time post injury greater than six months
Innervated and excitable lower extremity and trunk musculature
Adequate social support and stability
Willingness to comply with follow-up procedures
Appropriate body habitus (height and weight within acceptable limits as determined by study physician)
Neurologically stable as determined by a physician

Exclusion Criteria

Significant fracture risk or history of spontaneous fractures
History of heterotopic ossification at the hip, knee, or ankle
Non-English speaking
Insufficient upper extremity function to use an assistive device (e.g. walker or cane)
Females who are pregnant
Current pressure injury that would be exacerbated by study activities
Uncontrolled spasticity that would interfere with study activities
Significant range of motion limitations that would compromise study activities
History of vestibular dysfunction, balance problems, or spontaneous falls
Disorder or condition that require MRI monitoring
Acute and/or untreated orthopedic issues that would prevent weight bearing or exercising implanted muscles such as a dislocation or fracture
Acute and/or chronic medical problems left untreated or not controlled that would increase risk by using stimulation such as cardiac abnormalities, immunological/pulmonary/renal/circulatory compromise
Uncontrolled diabetes or hypertension
Presence of a demand pacemaker, cardiac defibrillator, or neuroprosthesis system with components in the legs
Any other medical or psychological condition that would be a contraindication Implant eligibility criteria • In addition to all of the above, the participant must be able to fully support their body weight in standing with an assistive device prior to implantation.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Cleveland?

Yes, this clinical trial (NCT06965127) has an active research site in Cleveland, OH that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Spinal Cord Injury (SCI) Treatment Options in Cleveland, OH

If you're searching for spinal cord injury (sci) treatment options in Cleveland, OH, this clinical trial (NCT06965127) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Cleveland research site is actively enrolling participants for this clinical trial. You'll receive care from experienced spinal cord injury (sci) specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all spinal cord injury (sci) clinical trials near you to find additional studies recruiting in your area.

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