Study Stopped
Recruitment is finished
Use of Neural Functional Electrical Stimulation for the Recovery of Grasping Movements for Patient With Quadriplegia.
1 other identifier
interventional
9
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2016
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 9, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 9, 2016
CompletedFirst Submitted
Initial submission to the registry
October 19, 2018
CompletedFirst Posted
Study publicly available on registry
October 26, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
June 15, 2019
CompletedFebruary 10, 2021
February 1, 2021
Same day
October 19, 2018
February 8, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Selectivity of stimulation
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.
a week
Interventions
A feasibility study consists of placing 2 electrodes around the radial or medial nerves intraoperatively. The movements caused by the electrical stimulation of these nerves are observed.
Eligibility Criteria
You may qualify if:
- Neurological level ≥ C7
- years old min and max 65 years old,
- Complete traumatic injury: defined by A or B score on the AIS scale.
- patient belonging to group 0 or 1 of the Giens classification.
- neurological stability (no change in muscle testing)\> 6 months,
- post-injury duration\> 6 months
- Patients undergoing surgery to restore elbow extension.
- 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.
- 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).
You may not qualify if:
- \. strong spasticity and contractures in flexion or extension of the upper limbs.
- \. Unstable epilepsy. 3. Unstable cardiovascular pathology (coronary heart disease, major hypertension, heart failure etc.).
- \. wearing a pacemaker. 5. Dermatological problems contraindicate the application of surface electrodes.
- \. body weight\> 100kg
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Clinique Beau Soleillead
- Institut National de la recherche en Informatique et Automatiquecollaborator
- University Hospital, Montpelliercollaborator
- Mxm-Obeliacollaborator
Study Sites (1)
Clinique Beau Soleil
Montpellier, 34070, France
Related Publications (1)
Tigra W, Dali M, William L, Fattal C, Gelis A, Divoux JL, Coulet B, Teissier J, Guiraud D, Azevedo Coste C. Selective neural electrical stimulation restores hand and forearm movements in individuals with complete tetraplegia. J Neuroeng Rehabil. 2020 May 19;17(1):66. doi: 10.1186/s12984-020-00676-4.
PMID: 32429963DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- DEVICE FEASIBILITY
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 19, 2018
First Posted
October 26, 2018
Study Start
February 9, 2016
Primary Completion
February 9, 2016
Study Completion
June 15, 2019
Last Updated
February 10, 2021
Record last verified: 2021-02