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NCT Number: NCT07139496

Combined Injury-site & Lumbosacral Epidural Spinal Cord Stimulation

Spinal cord stimulation (SCS) has been shown in previous studies to be capable of restoring motor and autonomic function in patients with chronic complete spinal cord injury (SCI). Clinical studies have demonstrated that SCS enables activation of previously paralyzed muscles, leading to functional improvements in patients in the chronic stage of paralysis through the delivery of activity-based interventions. For most previous studies on SCS in SCI, stimulation was invariably applied to lumbrosacral plexus only. In this study, after signing the consent form, the patient will be assigned for standard surgery with additional implant of the spinal cord stimulator. The investigators propose to conduct the SCS with three phases. For the first phase, SCS over lumbrosacral spinal cord will be activated for 3 months with appropriate stimulation of lower limb muscles for walking together with physiotherapy of individual muscle groups for walking. For the second phase, SCS over lumbrosacral spinal cord will be stopped. SCS over the injury site will be activated for 3 months with appropriate stimulation of lower limb muscles. For the third phase, SCS over both lumbrosacral spinal cord and injury site of spinal cord will be activated for another 3 months with appropriate stimulation of lower limb muscles.

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Key information

Conditions

Spinal Cord Injuries (SCI) Central Nervous System Diseases Nervous System Diseases Spinal Cord Diseases Spinal Cord Injuries Trauma, Nervous System Wounds and Injuries

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Spinal cord injury (SCI) causes damage to motor, sensory, and autonomic function below the level of injury. This can have a huge impact on the daily function of the patients, with devastating effects on their quality of life, especially those with paralysis. Surgical treatment including decompression surgery is an option to improve the neurological outcome of these patients if the paralysis or limb weakness were surgically correctable. However, even with surgical treatment, there are still many patients with residual neurological deficits, which may greatly impair their activities of daily living. Patients with post-SCI may also develop chronic debilitating pain, because of neurophysiological changes in the somatosensory system.

Spinal cord stimulation (SCS) has increasingly been used as a potential method of improving motor function and for pain relief in patients with spinal cord injury. SCS is a well-established therapeutic treatment with robust evidence, in the management of chronic neuropathic and ischaemic pain syndromes, including persistent back pain after surgery, complex regional pain syndrome, and chronic ischemic pain condition. Its proposed mechanism of analgesic effects includes the gate control theory of pain, and enhancement of GABAergic systems of dorsal horn cells by stimulating their dendrites. Currently, there is a lack of mechanistic studies of SCS for SCI pain and its effectiveness is not well established.

SCS has been shown in previous studies to be capable of restoring motor and autonomic function in patients with chronic complete spinal cord injury. Clinical studies have demonstrated that SCS enables activation of previously paralyzed muscles, leading to functional improvements in patients in the chronic stage of paralysis through the delivery of activity-based interventions. For most previous studies on SCS in SCI, stimulation was invariably applied to lumbrosacral plexus only. The proposed mechanism for the effects of relate to the increased excitability of the central pattern generators (CPG) and enhance tonic and rhythmic motor patterns in persons after SCI and results in the activation of lower extremity muscles for standing and stepping with and without assistive devices. It was also shown that SCS in combination with locomotor training provides sensorimotor training of the spinal circuitry and facilitates standing stepping to enhance neuroplasticity.

In this study the investigators hypothesize that the application of SCS to the injury site can provide a neuromodulatory effect to the recovering neurons, allowing for improved neurological function caudal to the injury site. The investigators propose to conduct a clinical trial to determine whether the application of SCS to both injury site and lumbrosacral spinal cord, instead of SCS over lumbrosacral spinal cord alone, can further improve motor function in patients with motor-complete subacute and chronic spinal cord injury. The investigators will also assess longer term secondary outcomes including lower limb functional scores, chronic pain, and health related quality of life.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • American Society of Anesthesiologist (ASA) status I-III
  • Age 18-70 years old
  • Patients with SCI more than 2 years
  • Traumatic or atraumatic spinal cord injury
  • American Spinal Injury Association (ASIA) Impairment Scale A and B
  • Have previous MRI to document extent of spinal cord injury before recruitment

Exclusion criteria

  • Chronic opioid user
  • Presence of chronic pain condition (pain duration over 3 months)
  • Alcohol or substance abuse
  • active and unaddressed psychiatric diseases

Treatment and study plan

Spinal cord stimulator

Device

After the implantation of the spinal cord stimulator, the study will begin with 3 phases:

For the first phase, SCS over lumbrosacral spinal cord will be activated for 3 months with appropriate stimulation of lower limb muscles for walking.

For the second phase, SCS over lumbrosacral spinal cord will be stopped. SCS over the injury site will be activated for 3 months with appropriate stimulation of lower limb muscles for walking.

For the third phase, SCS over both lumbrosacral spinal cord and injury site of spinal cord will be activated for another 3 months with appropriate stimulation of lower limb muscles for walking

During all the phrases, physiotherapy of individual muscle groups for walking will be arranged. Exoskeleton training will also be arranged for 4 to 5 hours per week.

Primary outcomes

  1. Assisted/independent standing or stepping (A/I) [Time Frame: Changes from baseline to the third phase of the intervention]

    Time frame: From baseline to three months after the third phase of the intervention.

    Assisted/independent standing or stepping of participants will be recorded, with 0 = unable, 1 = maximal assistance, 2 = moderate assistance, 3 = independent with device, 4 = fully independent.

  2. Gait analysis (GA) [Time Frame: Changes from baseline to the third phase of the intervention]

    Time frame: From baseline to three months after the third phase of the intervention.

    The participants' hip, knee range of motion will be recorded. The walking speed will also be recorded.

  3. Overground walking (OGW) [Time Frame: Changes from baseline to the third phase of the intervention]

    Time frame: From baseline to three months after the third phase of the intervention.

    The speed, time and distance for the participants' overground walking will be recorded.

  4. Treadmill stepping/ walking (TSW) [Time Frame: Changes from baseline to the third phase of the intervention]

    Time frame: From baseline to three months after the third phase of the intervention.

    The maximum tolerated speed (m/s) and duration (minutes) for treadmill stepping/walking will be recorded.

  5. Walking Index for Spinal Cord Injury Scale (WISCI 2) [Time Frame: Changes from baseline to the third phase of the intervention]

    Time frame: From baseline to three months after the third phase of the intervention.

    A score from 0 to 20 will be recorded for WISCI II. Level 0: "patient is unable to stand and/or participate in assisted walking" to level 20: "ambulates with no devices, no braces and no physical assistance, 10 meters".

  6. Sensory assessments of the lower limbs [Time Frame: Changes from baseline to the third phase of the intervention]

    Time frame: From baseline to three months after the third phase of the intervention.

    The sensory changes of the participants will be recorded with 'absent', reduced' or 'present'.

Secondary outcomes

  1. Pain Intensity [Time Frame: Changes from baseline to the third phase of the intervention]

    Time frame: From baseline to three months after the third phase of the intervention.

    NRS pain scores with movement will be recorded (NRS scale 0-10, where 0 is no pain, and 10 is the worst possible pain)

  2. Quality of Life [Time Frame: Changes from baseline to the third phase of the intervention]

    Time frame: From baseline to three months after the third phase of the intervention.

    A SF36 questionnaire with scores range from 0 to 100 for eight domains will be recorded, with a higher score defining a more favorable health state. The eight domains include: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions.

  3. Psychological Symptoms [Time Frame: Changes from baseline to the third phase of the intervention]

    Time frame: From baseline to three months after the third phase of the intervention.

    The Depression and Anxiety Symptom Stress Scale (DASS) of participants will be recorded. A score range from 0 to 42 in depression, anxiety and stress will be recorded with a higher score meaning a more severe psychological symptom.

  4. Presence of neuropathic pain [Time Frame: Changes from baseline to the third phase of the intervention]

    Time frame: From baseline to three months after the third phase of the intervention.

    A score of 3 or higher from an Identification Pain Questionnaire will be used to indicate the likely presence of neuropathic pain.

Study contacts

Contact information is provided by the study sponsor or research team.

Timmy CW Chan, MBBS

CONTACT

[email protected]

(852)22555679

Sponsors and collaborators

Lead sponsor

The University of Hong Kong

Other

Registry information

Official study title

Combined Injury-site & Lumbosacral Epidural Stimulation for Spinal Cord Injury - a Pilot Study.

Important dates

Study start
2025
Primary completion
2028
Study completion
2029
First posted
Aug 24, 2025
Registry last updated
Dec 1, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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