Evaluating Safety and Feasibility of Transcutaneous Spinal Cord Stimulation Following Traumatic and Non-Traumatic Spinal Cord Injury: A Pilot Study

NCT ID: NCT06520020

Last Updated: 2025-06-06

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-10-23
• Study Completion Date: 2026-06-30

Brief Summary

The study will be a non-randomized, non-blinded pilot study to analyze the safety and feasibility of a non-significant risk device, transcutaneous spinal cord stimulation. The aim is to include 30 total patients, 10 patients in each of 3 groups:

1. Non-traumatic spinal cord injury (ntSCI) with diagnosis of degenerative cervical myelopathy and offered surgical intervention.

2. Early tSCI screened during the hospital admission when cervical/thoracic spinal injury was diagnosed.

3. Delayed tSCI (control) screened 6-24 months after acute cervical/thoracic spinal injury.

Detailed Description

Spinal cord injury (SCI) can result from primary physical insults such as acute trauma, or secondary insults that result from chronic compression and ischemia. The resultant neurological impairment leads to high personal and societal burden. There are few effective therapies to improve function for those living with SCI. Spinal cord stimulation (SCS) represents a safe and potentially effective treatment for persons with SCI-related pain and paralysis. The aim of this study is to investigate the potential clinical utility of SCS delivered transcutaneously in patients at various stages of SCI, resulting from traumatic and non-traumatic mechanisms. This study will evaluate the ability to safely stimulate the injured spinal cord at defined intervals and record autonomic and sensorimotor function of participants across their admission, rehabilitation, and clinical follow-up.

Various upper and lower extremity-related functional measures will be assessed at baseline and at established follow-up timepoints across a 12-month period. The safety of this intervention, and the utility of each outcome measure will be the primary outcome of the study. To our knowledge, there are no reported clinical trials that have evaluated multi-modal outcomes of SCS. Furthermore, there are no proposed trials of SCS for these SCI subtypes across the post-injury spectrum posted to the platform clinicaltrials.gov. Data obtained from this pilot evaluation will be used to inform an early phase Ib/II trial of efficacy for improvement of paralysis, autonomic dysfunction, and pain following SCI.

Over 2.5 million Americans are living with various forms of SCI, equating to substantial individual and societal burden (1). Acute traumatic SCI average costs alone range from $380K to $1.4M. This high socioeconomic impact has undergone significant inflation with estimated annual costs of $4 billion in 1990, recently increasing to $23 billion. Approximately 13,000 new traumatic SCI events are noted yearly in North America. Degenerative cervical myelopathy (DCM) represents the most prevalent etiology of nontraumatic spinal cord (ntSCI) and dysfunction in adults. The prevalence of ntSCI is order(s) of magnitude higher than that of tSCI.

Together, these conditions significantly impact millions of North Americans often with greater personal impact that chronic conditions such as diabetes or cardiac disease. The considerable societal concern due to this individual disability is compounded by the lack of viable treatment options.

DCM arises from age-related degenerative processes, leading to osteophyte development, facet joint enlargement, ossification of spinal ligaments, and disk protrusion. These arthritic changes collectively compress the spinal cord causing injury with associated ischemia and inflammation. In turn, a similar constellation of symptoms develop including extremity pain, reduced motor function, numbness, hemodynamic lability, urinary incontinence, bowel dysfunction, and walking instability contributing towards higher years lived with disability (DALYs) as well as overall economic burden.

Currently, effective evidence-proven treatments are restricted to surgical decompression and rehabilitation. Narrative studies have shown that patients living with paralysis want options for neural modulation therapies, as they perceive the risk-to-benefit ratio of implanted devices more favorably than healthcare professionals. Given overall suboptimal outcomes in patients with SCI, it is critical to further enhance both the recovery rates and the extent of recovery beyond what is achievable through surgical decompression.

Spinal cord stimulation has been shown to mediate functional improvement following acute traumatic SCI in terms of limb function, ambulation, hand strength, autonomic dysfunction, intractable pain, and bladder control. The majority of published studies have applied stimulation during the chronic phase of recovery, and largely in a single or small group of participants.

Variable applications of SCS for SCI have yet to be demonstrated using multi-modality stimulation, such as spinal transcutaneous, spinal epidural, and transcranial magnetic stimulation of the motor cortex. Harkema and colleagues demonstrated that epidural SCS can return volitional motor control in participants who had none following chronic thoracic injury. Their work at the University of Louisville also has shown that multilevel transcutaneous spinal cord stimulation can be applied to several cervicothoracic regions spanning across the entire limb enlargement, and provide sensorimotor functional improvements during neurorehabilitation. These approaches have subsequently been applied at other centers with success for sensorimotor recovery.

The utilization of SCS in managing Failed Back Surgery Syndrome (FBSS), Complex Regional Pain Syndrome (CRPS), and chronic leg ischemia has been well documented. However, there is limited evidence indicating the use of SCS in patients with tSCI or ntSCI with regards to improving motor functions. This application of SCS could identify important differentiators in neural modulation that will correspond to improved functional outcomes, patient reported outcome measures (PROM), and quality of life (QoL). Should differentiators be observed, these conclusions will inform phase Ib/II study of SCS-based neuromodulation vs standard-of-care rehabilitation. This is directly in line with the best-of-practice and goals promoted by the leaders in SCI clinical research and patient-driven goals.

To date, there are no reported clinical trials involving participants in the subacute phase of tSCI, despite the widely-held belief that this phase offers the greatest potential for therapeutic intervention to reduce secondary injury and preserve functional networks.

Likewise, there are no clinical trials examining the role of perioperative SCS in patients diagnosed with any form of ntSCI (including patients with DCM who undergo surgical decompression).

The proposed study will directly address whether neuromodulation has a specific therapeutic potential for persons having sustained acute traumatic and non-traumatic spinal injuries. This study will specifically address whether this can be achieved with a non-significant risk device such as transcutaneous spinal cord stimulation. Lastly, this study will comparatively assess the modalities that can be used to reliably stimulate and measure the physiologic effects of neuromodulation of the injured spinal cord.

Additionally, this study aims to test the hypothesis that transcutaneous electrical spinal cord stimulation has equivalent modulatory effect on sensorimotor pathways and spinal cord function. This study will prospectively record neurologic outcomes to fully leverage the technologies at our disposal and maximize the potential benefit for each participant. The subsequent results will further help determine whether spinal cord neuromodulation can be directly correlated to either patient reported outcome or functional performance measures. Moreover, to determine feasibility of transcutaneous SCS at various timepoints after presentation, this study will measure spinal signal outputs before and after standard-of-care treatments including surgery and intensive neural rehabilitation.

The preliminary data in support of SCS for individuals with tSCI applied at chronic recovery phases has demonstrated promising outcomes, potentially ameliorating this severe condition. The investigation into utilizing SCS as a management approach for acute tSCI and ntSCI (ie. DCM), in conjunction with surgical interventions and rehabilitation, represents a promising prospect for enhancing the quality of life of those afflicted with this debilitating neurological disorder.

Conditions

Spinal Cord Stimulation; Electric Stimulation Therapy; Traumatic Spinal Cord Injury; Cervical Myelopathy

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Non-Traumatic Spinal Cord Injury (ntSCI,) DCM - Progressive

Non-traumatic spinal cord injury (ntSCI) with diagnosis of degenerative cervical myelopathy (DCM) and offered surgical intervention. Prospective.

Group Type: EXPERIMENTAL

Transcutaneous Spinal Cord Stimulation (Tc-SCS)

Intervention Type: DEVICE

This study will employ a DS8R Biphasic Constant Current Stimulator (Digitimer, Hertfordshire, United Kingdom) to administer transcutaneous (Tc) SCS through bursts of biphasic rectangular pulses, each lasting 400 μs to 1 ms, at 30 Hz frequency on a carrier frequency is 10 kHz. The intensity of stimulation will be 120% the threshold intensity that elicits visible twitch or motor evoked potential (MEP) triggered in the biceps brachii (BB) or abductor pollicis brevis (APB) muscle for upper extremity, and quadriceps femoris (QF) or tibialis anterior (TA) in the lower extremity.

Traumatic Spinal Cord Injury (tSCI) - Early/Acute

Traumatic spinal cord injury (tSCI) screened during the hospital admission when cervical/thoracic spinal injury was diagnosed. 2-6 weeks after injury.

Group Type: EXPERIMENTAL

Transcutaneous Spinal Cord Stimulation (Tc-SCS)

Intervention Type: DEVICE

This study will employ a DS8R Biphasic Constant Current Stimulator (Digitimer, Hertfordshire, United Kingdom) to administer transcutaneous (Tc) SCS through bursts of biphasic rectangular pulses, each lasting 400 μs to 1 ms, at 30 Hz frequency on a carrier frequency is 10 kHz. The intensity of stimulation will be 120% the threshold intensity that elicits visible twitch or motor evoked potential (MEP) triggered in the biceps brachii (BB) or abductor pollicis brevis (APB) muscle for upper extremity, and quadriceps femoris (QF) or tibialis anterior (TA) in the lower extremity.

Traumatic Spinal Cord Injury (tSCI) - Chronic

Delayed traumatic spinal cord injury (tSCI) screened 6-24 months after acute cervical/thoracic spinal injury. The use of transcutaneous spinal cord stimulation (Tc-SCS) in chronic SCI delivered in the delayed timeframe is relatively well studied, and therefore will serve as the control arm.

Group Type: ACTIVE_COMPARATOR

Transcutaneous Spinal Cord Stimulation (Tc-SCS)

Intervention Type: DEVICE

This study will employ a DS8R Biphasic Constant Current Stimulator (Digitimer, Hertfordshire, United Kingdom) to administer transcutaneous (Tc) SCS through bursts of biphasic rectangular pulses, each lasting 400 μs to 1 ms, at 30 Hz frequency on a carrier frequency is 10 kHz. The intensity of stimulation will be 120% the threshold intensity that elicits visible twitch or motor evoked potential (MEP) triggered in the biceps brachii (BB) or abductor pollicis brevis (APB) muscle for upper extremity, and quadriceps femoris (QF) or tibialis anterior (TA) in the lower extremity.

Interventions

Transcutaneous Spinal Cord Stimulation (Tc-SCS)

This study will employ a DS8R Biphasic Constant Current Stimulator (Digitimer, Hertfordshire, United Kingdom) to administer transcutaneous (Tc) SCS through bursts of biphasic rectangular pulses, each lasting 400 μs to 1 ms, at 30 Hz frequency on a carrier frequency is 10 kHz. The intensity of stimulation will be 120% the threshold intensity that elicits visible twitch or motor evoked potential (MEP) triggered in the biceps brachii (BB) or abductor pollicis brevis (APB) muscle for upper extremity, and quadriceps femoris (QF) or tibialis anterior (TA) in the lower extremity.

Intervention Type: DEVICE

Other Intervention Names

Electrical Stimulation

Eligibility Criteria

Inclusion Criteria

• Age: = 18 years and = 80 years.
• Written informed consent by patient and/or legal authorized representative (LAR).
• No other life-threatening condition.
• No evidence of sepsis.
• No evidence of superficial skin infection at site of surgery and intervention.
• An established diagnosis of either:

• cervical myelopathy with modified Japanese Orthopaedic Association score of 8-14, or
• acute cervical / thoracic SCI with ASIA Impairment Scale grade A-D (as assessed within 72 hours of injury) with neurologic level of injury (NLI) from C2 to T12.
• The ability to undergo, or have had, surgical intervention. -. The ability to undergo transcutaneous intervention including study procedures in the posterior cervical or thoracic midline at or after 14 days from surgery.

Exclusion Criteria

• Any concomitant impairment of the upper and lower limb at baseline that could potentially confound the neurologic assessments; including but not limited to traumatic or disease conditions like brachial plexus injury, peripheral neuropathy, spinal hematoma, transverse myelitis, non-compressive myelopathy, dementia, and Parkinson's disease.
• mJOA of >= 15 and <= 7, or AIS grade E tSCI at baseline assessment.
• Currently involved in another non-observational ntSCI or tSCI study, or receiving another interventional drug, that could interfere with recordings and confound adverse events.
• Other illness (including mental disorder) that could preclude accurate medical and neurological evaluation, at discretion of the treating surgeon and/or principal investigator.
• Unable to commit to the follow-up schedule.
• Recent history of regular substance abuse (illicit drugs, alcohol), which in the opinion of the investigator would interfere with the subject's participation in the study.
• Any condition likely to result in the patient's death within the next 12 months.
• Prisoner.
• Pregnancy.
• Cardiac pacemaker dependent, unable to undergo electrical stimulation.
• Brain implant, skull prosthesis, plate and screws limiting transcranial stimulation.
• Tattoo at site of skin electrode that causes heat/pain during stimulation.
• Subjects who in the opinion of the investigator are not suitable for inclusion in the study, with reason documented.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Francis Farhadi

OTHER

Sponsor Role: lead

Responsible Party

Francis Farhadi

Associate Professor, Neurosurgery

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Jared Wilcox, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Kentucky Neurosurgery

Locations

University of Kentucky - Chandler Medical Center

Lexington, Kentucky, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

H. Francis Farhadi, MD, PhD

Role: CONTACT

francis.farhadi@uky.edu

859-323-5661

Kris P Dyer, MPH, BS

Role: CONTACT

kris.dyer@uky.edu

859-323-4533

Facility Contacts

Francis H Farhadi, MD, PhD

Role: primary

francis.farhadi@uky.edu

859-562-0247

Kris P Dyer, MPH, BS

Role: backup

kris.dyer@uky.edu

859-323-4533

Other Identifiers

96620

Identifier Type: -

Identifier Source: org_study_id