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Human Factor Validation of Pediatric Mobility Device

NCT03714256 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 33

Last updated 2021-01-14

Study results available
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Summary

The purpose of this study is to validate the user interface of a pediatric power mobility device by establishing that the product is safe and effective use for the intended users.

Conditions

  • Disability Physical

Interventions

DEVICE

Device, patient mobility, powered

Pediatric mobility device

Sponsors & Collaborators

  • Permobil, Inc.

    lead INDUSTRY

Principal Investigators

  • Karin Leire · Permobil Group

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
6 Months
Max Age
36 Months
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-09-21
Primary Completion
2018-11-19
Completion
2018-11-19
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 NCT03714256 on ClinicalTrials.gov