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Motor, Sensory, and Autonomic Function in Traumatic Spinal Cord Injury After the LION Procedure. (SCI-LION)

Primary Purpose

Spinal Cord Injuries

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
LION procedure
NMES
Sponsored by
Spinal Cord Injury Centre of Western Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spinal Cord Injuries

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Willing and able to give informed consent for participation in the clinical investigation, and to comply with all requirements of the clinical investigation
  2. Traumatic SCI with:

    • neurological level below T5 and above L2
    • American Spinal Injury Association Impairment Grade A or B
    • spasticity in one or both lower extremities
    • Injury prior at least 12 months prior to enrollment

Exclusion Criteria:

  1. Female subject who is pregnant/planning pregnancy during the clinical investigation.
  2. Previous surgery/procedures interfering with the LION procedure incl. the presence of other implanted medical devices.
  3. Any other significant disease or disorder which, in the opinion of the Investigator, may either put the subject at risk because of participation in the clinical investigation, or may influence the result of the clinical investigation, or the subject's ability to participate in the clinical investigation

Sites / Locations

  • Helge Kasch

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Intervention

Control

Arm Description

All participant in the intervention group will undergo the LION procedure and subsequent neurostimulation.

All participants in the control group will be issued with a device for neuromuscular electrical stimulation.

Outcomes

Primary Outcome Measures

Improvement/change in walking capacity
Walking index for spinal cord injury, second revision (WISCI II)

Secondary Outcome Measures

Change in lean body mass
Changes in lean body mass on dual-energy x-ray absorptiometry
Change in distal motor latency of motor nerve conduction studies
Preoperative to postoperative change in distal motor latency of the compound muscle action potential.
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.
Change in muscle microarchitecture
Preoperative to postoperative changes in fiber-type composition on histochemical analysis of soles muscle biopsies.
Change in muscle motor unit number
Preoperative to postoperative changes in motor unit number estimation.
Change in compound muscle action potential scans.
Preoperative to postoperative changes in compound muscle action potential scan slope.
Change in sensory nerve action potential latency of sensory nerve conduction studies
Preoperative to postoperative change in sensory nerve action potential latency.
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.
Change in sensory discrimination
Change in parameters of quantitative sensory testing applying method of limits.
Change in bowel function
Changes in scores on the international spinal cord injury data set - bowel function
Change in bladder function
Changes in scores on the international spinal cord injury data set - lower urinary tract function
Change in health-related quality of life
Changes in scores of the international spinal cord injury data set - quality of life
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.
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.
Change in spasticity
Changes in scores of the modified Tardieu Scale for spasticity; scores 0-4, 4 being maximum level of spasticity.

Full Information

First Posted
January 24, 2018
Last Updated
September 22, 2021
Sponsor
Spinal Cord Injury Centre of Western Denmark
Collaborators
Aarhus University Hospital, Regionshospitalet Viborg, Skive, University of Southern Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT03441256
Brief Title
Motor, Sensory, and Autonomic Function in Traumatic Spinal Cord Injury After the LION Procedure.
Acronym
SCI-LION
Official Title
Motor, Sensory, and Autonomic Function After Laparoscopic Implantation of Neuroprosthesis - a Randomized Controlled Trial of the LION Procedure in Traumatic Spinal Cord Injury
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
January 1, 2018 (Actual)
Primary Completion Date
December 31, 2020 (Actual)
Study Completion Date
December 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Spinal Cord Injury Centre of Western Denmark
Collaborators
Aarhus University Hospital, Regionshospitalet Viborg, Skive, University of Southern Denmark

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Injuries

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
All participant in the intervention group will undergo the LION procedure and subsequent neurostimulation.
Arm Title
Control
Arm Type
Active Comparator
Arm Description
All participants in the control group will be issued with a device for neuromuscular electrical stimulation.
Intervention Type
Device
Intervention Name(s)
LION procedure
Other Intervention Name(s)
Neurostimulation
Intervention Description
Laparoscopic implantation of an impulse generator and four leads for electrical stimulation of femoral and sciatic nerves.
Intervention Type
Device
Intervention Name(s)
NMES
Other Intervention Name(s)
Neuromuscular electrical stimulation
Intervention Description
Conventional neuromuscular electrical stimulation via surface electrodes.
Primary Outcome Measure Information:
Title
Improvement/change in walking capacity
Description
Walking index for spinal cord injury, second revision (WISCI II)
Time Frame
Baseline, 3 mo., 6 mo., 9 mo., 12 mo.
Secondary Outcome Measure Information:
Title
Change in lean body mass
Description
Changes in lean body mass on dual-energy x-ray absorptiometry
Time Frame
Baseline, 12 mo.
Title
Change in distal motor latency of motor nerve conduction studies
Description
Preoperative to postoperative change in distal motor latency of the compound muscle action potential.
Time Frame
Baseline, 12 mo.
Title
Change in peak-peak amplitude of motor nerve conduction studies
Description
Preoperative to postoperative change in change in peak to peak amplitude of the compound muscle action potential.
Time Frame
Baseline, 12 mo.
Title
Change in muscle microarchitecture
Description
Preoperative to postoperative changes in fiber-type composition on histochemical analysis of soles muscle biopsies.
Time Frame
Baseline, 12 mo.
Title
Change in muscle motor unit number
Description
Preoperative to postoperative changes in motor unit number estimation.
Time Frame
Baseline, 12 mo.
Title
Change in compound muscle action potential scans.
Description
Preoperative to postoperative changes in compound muscle action potential scan slope.
Time Frame
Baseline, 12 mo.
Title
Change in sensory nerve action potential latency of sensory nerve conduction studies
Description
Preoperative to postoperative change in sensory nerve action potential latency.
Time Frame
Baseline, 12 mo.
Title
Change in peak-peak amplitude of the sensory nerve action potential of sensory nerve conduction studies
Description
Preoperative to postoperative change in peak-peak amplitude of the sensory nerve action potential.
Time Frame
Baseline, 12 mo.
Title
Change in sensory discrimination
Description
Change in parameters of quantitative sensory testing applying method of limits.
Time Frame
Baseline, 12 mo.
Title
Change in bowel function
Description
Changes in scores on the international spinal cord injury data set - bowel function
Time Frame
Baseline, 12 mo.
Title
Change in bladder function
Description
Changes in scores on the international spinal cord injury data set - lower urinary tract function
Time Frame
Baseline, 12 mo.
Title
Change in health-related quality of life
Description
Changes in scores of the international spinal cord injury data set - quality of life
Time Frame
Baseline, 12 mo.
Title
Change in quality of life
Description
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.
Title
Change in pain
Description
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.
Title
Change in spasticity
Description
Changes in scores of the modified Tardieu Scale for spasticity; scores 0-4, 4 being maximum level of spasticity.
Time Frame
Baseline, 12 mo.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Willing and able to give informed consent for participation in the clinical investigation, and to comply with all requirements of the clinical investigation Traumatic SCI with: neurological level below T5 and above L2 American Spinal Injury Association Impairment Grade A or B spasticity in one or both lower extremities Injury prior at least 12 months prior to enrollment Exclusion Criteria: Female subject who is pregnant/planning pregnancy during the clinical investigation. Previous surgery/procedures interfering with the LION procedure incl. the presence of other implanted medical devices. Any other significant disease or disorder which, in the opinion of the Investigator, may either put the subject at risk because of participation in the clinical investigation, or may influence the result of the clinical investigation, or the subject's ability to participate in the clinical investigation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Helge Kasch, MD
Organizational Affiliation
Spinal Cord Injury Centre of Western Denmark
Official's Role
Study Director
Facility Information:
Facility Name
Helge Kasch
City
Viborg
State/Province
Midtjylland
ZIP/Postal Code
8800
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Individual participant data may be requested by other researchers. Approvals from the Danish Data Protection Agency and individual participants will be required before data may be shared.
Links:
URL
http://www.nature.com/articles/s41393-021-00693-7
Description
Effect of pelvic laparoscopic implantation of neuroprosthesis in spinal cord injured subjects: a 1-year prospective randomized controlled study
URL
http://doi.org/10.5005/jp-journals-10033-1450
Description
Surgical Aspects of the Possover LION Procedure: An Emerging Procedure for Recovery of Visceral Functions and Locomotion in Paraplegics

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Motor, Sensory, and Autonomic Function in Traumatic Spinal Cord Injury After the LION Procedure.

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