DExterous Hand Control Through Fascicular Targeting (DEFT) - (Human Subjects)

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-95
SponsorUniversity of Texas Southwestern Medical Center

About this trial

Our goal is to temporarily implant the following groups for 540 +/- 30 days:

1. Forearm FAST electrodes

1. Five human partial hand amputees (amputated at the level of the hand) with 2 FAST electrodes in the ulnar nerve and 2-5 FAST electrodes in the median nerve. 2. Five human hand and forearm amputees (amputated at the level of the forearm) with 2 FAST electrodes in the ulnar nerve and 2-5 FAST electrodes in the median nerve . 2. Arm FAST electrodes

1. Five human partial hand amputees (amputated at the level of the hand) with 2 FAST electrodes in the ulnar nerve and 2-5 FAST electrodes in the median nerve. 2. Five human hand and forearm amputees (amputated at the level of the forearm) with 2 FAST electrodes in the ulnar nerve and 2-5 FAST electrodes in the median nerve. 3. Five human hand, forearm and arm amputees (amputated at the level of the arm) with 2 FAST electrodes in the ulnar nerve and 2-5 FAST electrodes in the median nerve.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male or female, age 18 and older, of any race or ethnicity

Able and willing to sign Consent

Able and willing to participate in all study activities including implantation, testing and explantation of the study device.

Able to communicate effectively in English without an interpreter

Disqualifiers

None

Trial design

Design model

Single group

Treatments tested in this trial

  • Fast electrode

    Other intervention

    Implant temporary Fast electrodes and record the nerve signals that control delicate finger motions and play back the nerve signals that give the hand feelings of touch and movement.

Treatment groups

25 Participants
are divided into 1 treatment group
Group A: Fast electrodesExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Motor Assessment

We will ask you to attempt to perform hand movements and positions. The movement trials will consist of simultaneous volitional movements and positioning of both the uninjured/sound limb and the injured/amputated "phantom" limb done. This allows us to have a physical record of exactly what movement is being attempted by the amputated limb. We will record nerve and muscle electrode activity during all of the movement trials. During some movement trials, we will stimulate the LIFE neural electrodes while recording from implanted vs. surface adhesive vs. percutaneous needle muscle electrodes

Time frame
up to 6 times per month beginning 2 days after implantation up to day 540 +/- 30 days
2

Sensory Assessment

We will also perform sensory detection and discrimination trials. Here, you will be asked to report if you detect any sensation during microstimulation (delivering very small electrical signals) via LIFE electrodes. If you do have a sensory perception, you will be asked to describe the quality and strength of the perception, e.g. location, touch, vibration, temperature. You may also be asked to fill out standardized sensory/pain assessments during microstimulation and after microstimulation is turned off. Other stimulation trials that may be done will include single or multiple electrode stimulation to see if subjects can perceive multiple sensory percepts simultaneously. Blinded trials may be done to determine if the subjects are actually perceiving the same percept for a given stimulation paradigm. Other trials may include modulating the stimulation parameters to determine if the sensory percept changes characteristics with varying stimulation paradigms.

Time frame
up to 6 times per month beginning 2 days after implantation up to day 540 +/- 30 days
3

Sensory-Motor Integration

After determining your sensory detection and discrimination parameters, we will ask you to repeat standardized assessments using the existing myoelectric partial hand prosthesis. Microstimulation via LIFE electrodes will be paired with motion or contact during task performance in order to determine whether providing evokes sensation during prosthesis use improves task-based performance.

Time frame
up to 6 times per month beginning 2 days after implantation up to day 540 +/- 30 days

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Texas Southwestern Medical Center

Lead sponsor

Defense Advanced Research Projects Agency

Collaborator

Nerves Incorporated, Inc.

Collaborator

Arizona State University

Collaborator

University of Minnesota

Collaborator