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Use of Neural Functional Electrical Stimulation for the Recovery of Grasping Movements for Patient With Quadriplegia.

Not Applicable
Terminated
Conditions
Spinal Cord Injuries
Registration Number
NCT03721861
Lead Sponsor
Clinique Beau Soleil
Brief Summary

Functional electrical stimulation (FES) has been used for decades in rehabilitation centers. Having demonstrated efficacy for prevention of muscle atrophy following spinal cord injury (SCI), FES can also be considered for functional restoration of hand movements in the patients with complete tetraplegia belonging to group 0 or 1 of the classification of Giens. However, the majority of the systems using the FES directly stimulates the muscles (surface electrodes, intramuscular or epimysial), which increases the number of components and requires more electrical energy for the muscle activation. Nerve stimulation would activate more muscles through a reduced number of electrodes, limiting the number of internal components, reduces the risk of spreading infections and require less electrical energy for its operation.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
9
Inclusion Criteria
  1. Neurological level ≥ C7
  2. 18 years old min and max 65 years old,
  3. Complete traumatic injury: defined by A or B score on the AIS scale.
  4. patient belonging to group 0 or 1 of the Giens classification.
  5. neurological stability (no change in muscle testing)> 6 months,
  6. post-injury duration> 6 months
  7. Patients undergoing surgery to restore elbow extension.
  8. threshold of stimulation and diffusion of the studied muscles below 50 mA of intensity for a pulse width of 300 μs and a frequency of 25 Hz.
  9. positive electrical mapping of muscles with a minimum score of 4 MRC for at least one of the extensors (triceps, ECRL, ECRB, EDC, EPL) and / or flexor (FPL, FDS, FDP).
Exclusion Criteria
    1. strong spasticity and contractures in flexion or extension of the upper limbs.

    2. Unstable epilepsy. 3. Unstable cardiovascular pathology (coronary heart disease, major hypertension, heart failure etc.).

    3. wearing a pacemaker. 5. Dermatological problems contraindicate the application of surface electrodes.

    4. body weight> 100kg

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Selectivity of stimulationa week

Electrical stimulation of the median or radial nerve via multipolar "cuff" electrodes induces electromyographic signals on a number of muscles.

If at least 92% of cases, it is possible to selectively stimulate 4 muscle groups (the elbow extensor: triceps, the extensors of the fingers and carp: ECRL, ECRB, EDP, EPL, the flexor of the thumb: FPL and flexors of 4 fingers (II to V): FDS and FDP) to restore 4 functions (elbow, wrist and finger extensions; the 4 fingers and the thumb flexions).

An activation of a muscle group is considered selective if both the selectivity index is ≥ 0.7 and the recruitment is ≥20%. Finally, there will be success the selective activation induces the right movements (extension of the elbow, extension of the wrist and fingers, flexion of the 4 fingers and flexion of the thumb). There will be failure otherwise.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Clinique Beau Soleil

🇫🇷

Montpellier, France

Clinique Beau Soleil
🇫🇷Montpellier, France
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