Cleveland, OHNCT06611748Now EnrollingIRB Ready

Spinal Cord Injury Cervical Clinical Trial in Cleveland, OH

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

Sponsored by MetroHealth Medical Center

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Expert Care in Cleveland

Access spinal cord injury cervical specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related spinal cord injury cervical treatment provided free

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Check if you qualify for this spinal cord injury cervical 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 Cervical Study in Cleveland

The purpose of this study is to evaluate a new method of restoring hand function to people with spinal cord injury. Current methods to restore hand function include tendon transfers and nerve transfers. This study will evaluate the grasp strength that can be achieved with a small, implantable stimulator. KeyGrip is an investigational device that works by activating paralyzed muscles with low levels of electrical current. The word "investigational" means the study device is still being tested in research studies and is not approved by the U.S. Food and Drug Administration (FDA) for the use being studied. Hypothesis. The study is designed to explore the feasibility of this approach; no hypothesis is planned at this stage

Sponsor: MetroHealth Medical Center

Who Can Participate

Inclusion Criteria

Male or female adults 18 years of age or older;
Cervical spinal cord injury as defined by: a) International Standard for Neurological Classification of Spinal Cord Injury motor level of C1 through C7; and b) American Spinal Injury Association Impairment Scale (AIS) grade A, B, or C;
Six months or more post-injury (neurostability);
Neurologically stable following any nerve transfers affecting the upper extremity (typically, one-year post-surgery);
Musculoskeletally and neurologically stable following any tendon transfers affecting the upper extremity (typically 6 months post-surgery).
Peripheral nerve innervation to upper extremity muscles, including Grade 3/5 or higher Stimulated Manual Muscle Testin at least two of the muscles in one arm:
Good proximal voluntary upper extremity strength as defined by biceps/ brachialis / brachioradialis strength of 2/5 or higher on Manual Muscle Testing the side intended for implantation;
Medically stable; and
Able to understand and provide informed consent;

Exclusion Criteria

Other neurological conditions (Multiple Sclerosis, diabetes with peripheral nerve involvement);
Associated peripheral nerve / brachial plexus injury;
Progressive Spinal Cord Injury;
Active implantable medical device (AIMD) such as a pacemaker or defibrillator;
Active untreated infection such as urinary tract infection or pneumonia;
Active pressure injury;
History of coagulopathy, HIV, cardiopulmonary disease, bradycardia, poorly controlled autonomic dysreflexia, or chronic obstructive pulmonary disease that would preclude safe participation in the trial as determined by the investigator;
Unhealed fractures that prevent functional use of arm;
Extensive upper extremity denervation (fewer than two excitable hand muscles);
Involvement in other ongoing clinical studies that exclude concurrent involvement in this study;
Currently pregnant (neuroprosthesis implantation delayed until no longer pregnant based on self-report); Urine or serum testing will happen during the pre-surgery evaluation.
Presence of disease that might interfere with participant safety, compliance, or evaluation of the condition under study;
Other significant medical findings that, in the opinion of the investigator, preclude safe participation in the trial

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 (NCT06611748) 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 Cervical Treatment Options in Cleveland, OH

If you're searching for spinal cord injury cervical treatment options in Cleveland, OH, this clinical trial (NCT06611748) 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 cervical 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 cervical clinical trials near you to find additional studies recruiting in your area.

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