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Myoelectric SoftHand Pro to Improve Prosthetic Function for People With Below-elbow Amputations: A Feasibility Study

NCT02274532 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 18

Last updated 2018-01-18

No results posted yet for this study

Summary

A study to investigate the hypothesis that a Pisa/IIT Robotic SoftHand Pro converted to a prosthetic terminal device will enhance the performance of people with limb loss in a wider range of daily living tasks than allowed by today's commercially available prosthetic hands, and will exceed established benchmarks for activities of daily living (ADL).

Conditions

  • Upper Limb Amputation Below Elbow (Injury)

Interventions

DEVICE

SoftHand

Biomechanical, ADL, and functional testing.

Sponsors & Collaborators

  • Arizona State University

    collaborator OTHER

  • University of Pisa

    collaborator OTHER

  • Karen L. Andrews, M.D.

    lead OTHER

Principal Investigators

  • Karen L. Andrews, M.D. · Mayo Clinic

Study Design

Allocation
NON_RANDOMIZED
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-10-24
Primary Completion
2016-05-17
Completion
2016-05-17

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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 NCT02274532 on ClinicalTrials.gov