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Implanted Myoelectric Control for Restoration of Hand Function in Spinal Cord Injury

NCT00583804 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2025-10-03

Study results available
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Summary

The purpose of this study is to evaluate the effectiveness of an implanted stimulator and sensor for providing hand and arm function for individuals with cervical level spinal cord injury.

Conditions

  • Spinal Cord Injury
  • Tetraplegia

Interventions

DEVICE

IST-12

Implanted stimulator and sensor device, with twelve implanted stimulating electrodes and two myoelectric signal recording electrodes.

Sponsors & Collaborators

  • Case Western Reserve University

    collaborator OTHER

  • VA Office of Research and Development

    collaborator FED

  • FDA Office of Orphan Products Development

    collaborator FED

  • MetroHealth Medical Center

    lead OTHER

Principal Investigators

  • Kevin L Kilgore, Ph.D. · MetroHealth Medical Center

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1989-04-01
Primary Completion
2015-01-01
Completion
2027-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00583804 on ClinicalTrials.gov