Neural Stimulation for Hand Grasp (AGILIS)

Assistance Publique - Hôpitaux de Paris

Status

Completed

Conditions

Quadriplegia

Treatments

Device: Neurostimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT04306328

APHP190280

Details and patient eligibility

About

A selective neural stimulation as the investigators propose allows to stimulate several muscles via a single electrode. Neural stimulation requires less energy for muscle activation. In our approach, 2 electrodes will be implanted above the elbow on the median and radial nerves. This considerably reduces the number of implanted elements and therefore i) the risk of infection, ii) the risk of failure, iii) the surgical risk through minimally invasive surgery.

Our main hypothesis is that multipolar neural electrical stimulation of the median nerve (flexion) and the radial nerve (extension) allows:

on the one hand, a selective, individualized motor activation (muscle by muscle)
on the other hand, a synergistic motor activation (association of several muscles) for the purpose of production of functional movements.

Full description

Electrical stimulation of the muscles has been used for decades in rehabilitation units specializing in the treatment of spinal cord injuries. It has been shown to be effective in building muscle and preventing muscle atrophy following spinal cord injury (SCI) or stroke. It can also be used to reduce spasticity and above all to promote functionally useful motor control. It is then a Functional Electric Stimulation (FES). In the quadriplegic person marked by a severe motor deficiency of the upper limbs, FES is today the only technique allowing to restore a functional gripping movements in the case where the active muscular resources below the elbows are missing or too weak to allow tendon transfer surgery.

Like "Freehand", all the devices using FES directly stimulate the muscles (surface, intramuscular or epimysial electrodes) and therefore require a high number of internal components with a theoretical risk of infection and greater rejection. since each muscle must be activated via an electrode (up to 12 in the case of "FreeHand"). The investigators propose instead selective neural stimulation as it allows stimulating several muscles via a single electrode. Neural stimulation requires less energy for muscle activation. In our approach, 2 electrodes will be implanted above the elbow on the median and radial nerves. This considerably reduces the number of implanted elements and therefore i) the risk of infection, ii) the risk of failure, iii) the surgical risk thanks to minimally invasive surgery. The procedure consisted of placing a multi-contact cuff electrode around the radial or median nerves and observing the effects of electrical neural stimulation in terms of muscle selectivity, force produced and movement induced. In a previous study, the investigators already proved through acute intra operative testing (under Ethics Committee approval, #NCT03721861) that:

No failure of the electrodes or of the stimulator was noted.
For all of the 8 subjects, it was possible to selectively stimulate muscle groups to obtain the opening of the thumb and fingers, or the flexion of the thumb, fingers and obtaining possibly functional grip like the forceps with opposition of the thumb or palmar grip.

A second feasibility study (Ethics committee registration #2016-A00711-50) with 17 quadriplegic patients assessed the subject's ability to use voluntary contractions of sus lesional muscles (EMG recordings in 8 subjects) or voluntary movements of shoulders (inertial recordings in 9 subjects) to control the movements of a robotic hand or the triggering of an electrical surface stimulation of the muscles of the forearm. All of the patients managed to master the proposed interface after a short familiarization period.

On the basis of the results of these two studies, the investigator wish to take an additional step in the development of a gripping assistance device for patients with spinal cord injury:

by proposing the implantation of two cuff electrodes with percutaneous connection on the arm of quadriplegic people. The electrodes will be kept in place for a period of 1 month before being definitively explanted. An implanted cable will connect the electrodes to an external connector.

Enrollment

2 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Informed consent signed
Patient affiliated to a social security (state medical aid excepted).
Neurological level ≥ C7
18 years old ≤ age ≤ 65 years old,
complete traumatic injury: defined by an A or B score on the AIS scale. (AIS A or - complete motor deficit under injury. This is an internationally agreed standard for describing spinal cord injury)
neurological stability (no change in muscle testing) > 6 months,
post-injury duration > 6 months
patients without active muscle resources for conventional tendon transfer surgery on the forearm and hand

Exclusion criteria

patient deprived of liberty (by judicial or administrative decision).
adult patient who is subject to a legal protection measure or unable to express consent
participation in another ongoing clinical trial
pregnant or breastfeeding women or women of childbearing age without effective contraception
spasticity and contractures in flexion or extension of the upper limbs of a destabilizing nature.
unstable epilepsy with a notion of a epileptic seizure that occurred within the previous 12 months.
unstable cardiovascular pathology (coronary heart disease, major hypertension, heart failure, etc.).
infectious pathology under treatment at the inclusion visit
wearing a pacemaker.
dermatological problems contraindicating the application of surface electrodes.
body weight >100 kg
psychiatric condition and/or history contraindicating participation in research
any contraindications to anesthesia and/or surgery
hypersensitivity to low molecular weight heparin (LMWH) or to any of the excipients of the specialty used
history of immune-mediated heparin-induced thrombocytopenia (HIT) within the last 100 days or presence of circulating antibodies
clinically significant active bleeding or a condition associated with a high risk of bleeding
electrical mapping identified as negative during the inclusion visit, i.e. with muscles revealing a rating < 4 MRC for at least one of the extensors (ECRL, ECRB, EDC, EPL) or one of the flexors (FPL, FDS, FDP).