Grasp-Release Assessment of a Networked Neuroprosthesis Device

Not Applicable

Recruiting

• Conditions: Spinal Cord Injury at C5-C7 Level; Spinal Cord Injuries; Spinal Cord Injury Cervical
• Interventions: Device: Networked Neuroprosthesis Device

• Registration Number: NCT05863754
• Lead Sponsor: MetroHealth Medical Center

Brief Summary

The overall objective of this trial is to characterize the safety and effectiveness of the Networked Neuroprosthesis Device - Upper Extremity (NP-UE) in individuals living with cervical SCI.

Detailed Description

The Networked Neuroprosthesis(NNP) is an implantable, configurable neuromodulation platform that provides functional movement by the coordinated activation of peripheral neural pathways activating innervated paralyzed muscles, and sensing of physiological signals. The NNP-UE Configuration activates nerves of the upper extremity (arm and hand), and senses voluntary motion and/or electromyogram (EMG) in order to provide hand grasp.

The proposed work is focused on restoration of hand and reaching functions for people with cervical level spinal cord injury. For individuals who have sustained this injury, restoration of hand function is their top priority, and existing alternatives are limited. Neuroprosthesis are the most promising method for significant gain in hand and arm function.

Study Timeline

• Study Start: 2022-01-23
• Study First Submitted: 2023-04-28
• Study First Submitted QC: 2023-05-08
• Study First Posted: 2023-05-18
• Status Verified: 2024-08
• Last Update Submitted: 2024-08-23
• Last Update Posted: 2024-08-27
• Primary Completion: 2026-12-01
• Study Completion: 2027-12-01

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 13

Inclusion Criteria

• Male or female, age > 16 years.

• Cervical level spinal cord injury, as defined by:

  1. International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI) motor level of C1 through C7 and
  2. American Spinal Injury Association (ASIA) Impairment Scale (AIS) grade A, B, or C;

• Six months or more post-injury (neurostability);

• Neurologically stable following any nerve transfers affecting the upper extremity (typically, one year post surgery);

• Musculoskeletally and neurologically stable following any tendon transfers affecting the upper extremity (typically, 6-months).

• Peripheral nerve innervation to upper extremity muscles, including a grade 3/5 or higher Stimulated Manual Muscle Test (SMMT) strength in at least two of the following muscles in one arm:

  1. Adductor Pollicus, Abductor Pollicus Brevis (AbPB), Flexor Pollicus Longus (FPL), Extensor Pollicus Longus (EPL)/Extensor Pollicus Brevis (EPB), Extensor Digitorum Communis (EDC), Flexor Digitorum Superficialis (FDS), Flexor Digitorum Profundus (FDP), Pronator Quadratus (PQ), Extensor Carpi Ulnaris (ECU), Extensor Carpi Radialis Brevis (ECRB), Extensor Carpi Radialis Longus (ECRL), Flexor Carpi Ulnaris (FCU), Flexor Carpi Radialis (FCR), First Dorsal Interosseous(1DI), triceps,
  2. At least two of the grade 3/5 or higher excitable muscles must also have grade 2/5 or lower voluntary strength;

• Good proximal upper extremity strength as defined by biceps/brachialis/brachioradialis strength of 2/5 or higher on Manual Muscle Test on the side intended for implantation;

• Medically stable;

• Able to understand and provide informed consent.

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Exclusion Criteria

• Other neurological conditions (MS(multiple Sclerosis), diabetes with peripheral nerve involvement); Associated peripheral nerve / brachial plexus injury
• Progressive SCI;
• Co-existing cervical spine pathology (syrinx, unstable segment)
• Active implantable medical device (AIMD) such as a pacemaker or defibrillator;
• Active untreated infection such as pressure injury, urinary tract infection, pneumonia;
• History of coagulopathy, HIV, cardiopulmonary disease, bradycardia, poorly controlled autonomic dysreflexia, or chronic obstructive pulmonary disease that would preclude safe participation in the trial as determined by the investigator;
• Unhealed fractures that prevent functional use of arm;
• Extensive upper extremity denervation (fewer than two excitable hand muscles);
• Involvement in other ongoing clinical studies that exclude concurrent involvement in this study;
• Disorder or condition that requires MRI monitoring;
• Mechanical ventilator dependency;
• Currently pregnant (neuroprosthesis implantation delayed until no longer pregnant);
• Presence of disease that might interfere with participant safety, compliance, or evaluation of the condition under study;
• Other significant medical findings that, in the opinion of the investigator, preclude safe participation in the trial.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Experimental: Intervention - implant neuroprosthesis	Networked Neuroprosthesis Device	Receives implanted networked neuroprosthetic system for arm and hand function. Undergoes functional training and assessment.

Primary Outcome Measures

Name	Time	Method
Change in Grasp-Release Test	Pre-implant and three months post-implant, 6 months post implant, 12 months post implant	Ability to pick up, move, and release six standard objects

Secondary Outcome Measures

Name	Time	Method
Change in Grasp Dynameter(force)	Pre-implant and three months post-implant, 6 months post implant, 12 months post implant	Measure of muscular strength or the maximum force/tension generated by one's forearm muscles.
Change in Activities of Daily Living (ADL) Abilities Test	Pre-implant and three months post-implant, 6 months post implant, 12 months post implant	The Activities of Daily Living (ADL) profile uses both observation and interview to assess function in tasks completed in the personal, home, and community environments.
Change in Canadian Occupational Performance Measure (COPM)	Pre-implant and three months post-implant, 6 months post implant, 12 months post implant	Evidence-based outcome measure designed to capture a client's self-perception of performance in everyday living, over time
Change in Spinal Cord Independence Measure III (SCIM-III)	Pre-implant and three months post-implant, 6 months post implant, 12 months post implant	The measure address three specific areas of function in patients with spinal cord injuries (SCI). It looks at self-care (feeding, grooming, bathing, and dressing), respiration and sphincter management, and a patient's mobility abilities (bed and transfers and indoors/outdoors)

Trial Locations

Locations (1)

MetroHealth Medical Center; 🇺🇸 Cleveland, Ohio, United States