Can an Array of Micro-electrodes Implanted in a Human Nerve Record Neural Signals and Provide Feedback?
NCT ID: NCT05505513
Last Updated: 2025-10-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
3 participants
INTERVENTIONAL
2020-12-21
2026-12-31
Brief Summary
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Detailed Description
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The HAPTIX System study will investigate the safety and efficacy of using electromyography (EMG), plus neural recording and nerve stimulation, to control and provide cutaneous and proprioceptive feedback from a dexterous, motorized and sensorized, upper-extremity prosthesis (e.g., the DEKA LUKE arm) used by amputees.
The HAPTIX System is intended to permit the function of an upper-extremity prosthesis to assist in activities of daily living (ADLs) using neurostimulation and recording of EMG and neural signals to control the prosthesis, and evoke touch sensation and proprioception in upper-extremity amputees with DEKA LUKE sensorized upper extremity prosthesis.
The HAPTIX System study is an early feasibility study (EFS) of the use of a combination of EMG recording electrodes, neural recording and stimulating electrodes, and external electronics and algorithms designed to provide sensory and proprioceptive feedback to the amputee, and to control movements of a prosthetic hand.
EMG signals from the residual forearm muscles of amputees will be recorded using up to 8 custom bipolar PermaLoc® electrodes. The incorporation of these electrodes into the HAPTIX System is described in 001\_G190131A002\_Amended\_Device Description. Nerve signals will also be recorded using up to 3 percutaneous Utah Slanted Electrode Arrays (pUSEAs), whose electrode tips will be implanted intrafascicularly in residual arm nerves. Present-version pUSEAs utilize a transcutaneous lead and extracorporeal connector. Motor signals from the nerve will contribute to decoding motor intents decoded to control an advanced prosthetic hand. Nerve stimulation to evoke sensory perceptions will be provided by passing current through individual pUSEA electrodes, separately or in combination.
Conditions
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Study Design
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NA
SINGLE_GROUP
DEVICE_FEASIBILITY
NONE
Study Groups
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Implantation of a percutaneous Utah Slanted Electrode Arrays (pUSEAs)
The arm (s) of the patient which has been amputated. Intervention include insertion of the percutaneous Utah Slanted Electrode Arrays which will interact with nerve endings in order to gain knowledge about device feasibility and nerve stimulation.
percutaneous Utah Slanted Electrode Arrays (pUSEAs)
Microelectrode slanted arrays with a large number of electrodes will be surgically implanted into peripheral nerves of patients with limb amputations.
Interventions
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percutaneous Utah Slanted Electrode Arrays (pUSEAs)
Microelectrode slanted arrays with a large number of electrodes will be surgically implanted into peripheral nerves of patients with limb amputations.
Eligibility Criteria
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Inclusion Criteria
* unilateral and bilateral traumatic or elective upper extremity amputations at the transradial level
Exclusion Criteria
* pregnancy
* inability to consent
* psychiatric comorbidity
* medical conditions that significantly increase the risk of adverse effects of general anesthesia
18 Years
65 Years
ALL
No
Sponsors
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University of Utah
OTHER
Responsible Party
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Douglas Hutchinson
Principle Investigator
Principal Investigators
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Douglas Hutchinson, M.D.
Role: PRINCIPAL_INVESTIGATOR
University of Utah Orthopaedics
Locations
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The University Orthopaedic Center
Salt Lake City, Utah, United States
Countries
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Central Contacts
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Facility Contacts
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Douglas Hutchinson, M.D.
Role: primary
Other Identifiers
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124231
Identifier Type: -
Identifier Source: org_study_id
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