Possover pioneered a minimally invasive and fully reversible laparoscopic technique, laparoscopic implantation of neuroprosthesis (LION), for precise placement of an implantable pulse generator and one to four leads for stimulating nerves of the lumbosacral plexus. Unexpectedly, Possover in 2014 made the clinical observation that four patients with complete and incomplete chronic traumatic spinal cord injury regained significant motor and sensory function following the LION procedure for bladder and bowel dysfunction. The primary objective of this randomized clinical trial is to investigate whether the LION procedure and the subsequent neurostimulation in individuals with chronic traumatic thoracolumbar spinal cord injury with spastic paraplegia is associated with increased walking capacity.
Sustaining a spinal cord injury impacts the mental and physical wellbeing of the injured individuals profoundly; quality of life suffers and subsequently the risk of suicide is greatly increased as compared to the general population. While spinal cord injury compromises an individual's mobility, dependency does not necessarily ensue; most individuals will require a wheelchair, braces or other assistive devices for maintaining activities of daily living and participating in society i.e. work, sport etc. Furthermore, individuals with spinal cord injury face numerous medical complications and reduced life expectancy as a direct result of their disability.Detrusor over-activity and sphincter dyssynergia are seen in up to 85% of cases and improved control of micturition and defaecation closely follows restoration of ambulation as primary rehabilitation goals of patients with spinal cord injury. Recovery after initial inpatient rehabilitation is at best modest and conversion rate of the American Spinal Injury Association Impairment Scale grade remain poor for grades A and B. Likewise, the rate of motor improvement stagnates over time leaving many patients with permanent motor, sensory and autonomic deficits. 9-12 months after their initial injury, most patients have essentially exhausted their possibility of further restorative treatments. Possover pioneered a minimally invasive and fully reversible laparoscopic technique, laparoscopic implantation of neuroprosthesis (LION), for precise placement of an implantable pulse generator and one to four leads for stimulating nerves of the lumbosacral plexus; a significant number cases suggest this technique is safe and efficacious in treating overactive and atonic bladder disturbances, neurogenic bowel dysfunction, and abdominopelvic neuropathic pain. Unexpectedly, Possover in 2014 made the clinical observation that four patients with complete and incomplete chronic traumatic spinal cord injury regained significant motor and sensory function following the LION procedure for bladder and bowel dysfunction. Expanding further on the topic, Possover have recently published an updated case series of 18 patients om whom 16 are now capable of weight bearing standing and 12 are furthermore capable of voluntary stepping. The primary objective of this randomized clinical trial is therefore to investigate whether the LION procedure and the subsequent neurostimulation in individuals with chronic traumatic thoracolumbar spinal cord injury with spastic paraplegia is associated with increased walking capacity.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
16
Laparoscopic implantation of an impulse generator and four leads for electrical stimulation of femoral and sciatic nerves.
Conventional neuromuscular electrical stimulation via surface electrodes.
Helge Kasch
Viborg, Central Jutland, Denmark
Improvement/change in walking capacity
Walking index for spinal cord injury, second revision (WISCI II)
Time frame: Baseline, 3 mo., 6 mo., 9 mo., 12 mo.
Change in lean body mass
Changes in lean body mass on dual-energy x-ray absorptiometry
Time frame: Baseline, 12 mo.
Change in distal motor latency of motor nerve conduction studies
Preoperative to postoperative change in distal motor latency of the compound muscle action potential.
Time frame: Baseline, 12 mo.
Change in peak-peak amplitude of motor nerve conduction studies
Preoperative to postoperative change in change in peak to peak amplitude of the compound muscle action potential.
Time frame: Baseline, 12 mo.
Change in muscle microarchitecture
Preoperative to postoperative changes in fiber-type composition on histochemical analysis of soles muscle biopsies.
Time frame: Baseline, 12 mo.
Change in muscle motor unit number
Preoperative to postoperative changes in motor unit number estimation.
Time frame: Baseline, 12 mo.
Change in compound muscle action potential scans.
Preoperative to postoperative changes in compound muscle action potential scan slope.
Time frame: Baseline, 12 mo.
Change in sensory nerve action potential latency of sensory nerve conduction studies
Preoperative to postoperative change in sensory nerve action potential latency.
Time frame: Baseline, 12 mo.
Change in peak-peak amplitude of the sensory nerve action potential of sensory nerve conduction studies
Preoperative to postoperative change in peak-peak amplitude of the sensory nerve action potential.
Time frame: Baseline, 12 mo.
Change in sensory discrimination
Change in parameters of quantitative sensory testing applying method of limits.
Time frame: Baseline, 12 mo.
Change in bowel function
Changes in scores on the international spinal cord injury data set - bowel function
Time frame: Baseline, 12 mo.
Change in bladder function
Changes in scores on the international spinal cord injury data set - lower urinary tract function
Time frame: Baseline, 12 mo.
Change in health-related quality of life
Changes in scores of the international spinal cord injury data set - quality of life
Time frame: Baseline, 12 mo.
Change in quality of life
Changes in the scores of the Short Form 36 questionnaire; the questionnaire has eight subscales (vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role functioning, and mental health). Each sub scale scores 0-100, 0 indicating maximal disability.
Time frame: Baseline, 12 mo.
Change in pain
Changes in the brief pain inventory questionnaire; questionnaire consists of 17-items addressing pain severity, pain location, pain chronicity, and amount of pain relief. Each item scores are 0-10, 10 indicating either maximum pain severity, maximum interference or maximum relief, respectively.
Time frame: Baseline, 3 mo., 6 mo., 9 mo., 12 mo.
Change in spasticity
Changes in scores of the modified Tardieu Scale for spasticity; scores 0-4, 4 being maximum level of spasticity.
Time frame: Baseline, 12 mo.
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