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Home Study of an Advanced Upper Limb Prosthesis

NCT01551420 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2019-04-30

Study results available
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Summary

The overall study objective is to examine the feasibility, acceptance, and benefits of home use of an advanced upper limb prosthetic device as well as the logistical support requirements utilized during 3 months of home usage. All participating subjects will enroll in Part A of the study which will involve supervised training. Eligible subjects will be invited to participate in Part B, the home use portion of the study.

Conditions

  • Traumatic Amputation of Arm

Interventions

DEVICE

Advanced upper limb prosthetic device IMU controlled

Advanced upper limb prosthetic IMU controlled

DEVICE

Advanced upper limb prosthetic EMG-PR controlled

Advanced upper limb prosthetic EMG-PR controlled

Sponsors & Collaborators

  • VA Office of Research and Development

    lead FED

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-04-01
Primary Completion
2017-12-19
Completion
2018-12-31
FDA Device
Yes

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 NCT01551420 on ClinicalTrials.gov