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NCT03714256

Human Factor Validation of Pediatric Mobility Device

Permobil, Inc.·ClinicalTrials.gov·device·Device trialCompleted
View on ClinicalTrials.gov →
Study focus
Disease/Condition
Disability Physical
Drug/Device/Intervention
Device, patient mobility, powered
Study type
Interventional
Intervention type
device
Sponsor & location
Primary sponsor
Permobil, Inc.
Location
Cincinnati,Corvallis,Nashville, United States of America
Timeline & enrollment
Phase
N/A
Start date
Sep 21, 2018
End date
Nov 19, 2018
Enrollment
33 participants
Primary outcome

Cumulative Number of Use Errors Associated With the Usage of the Device According to Labelling

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.

ICD-10 classifications
Other physical therapyLimitation of activities due to disabilityDependence on wheelchairPostprocedural musculoskeletal disorders, not elsewhere classifiedFamily history of other disabilities and chronic diseases leading to disablement, not elsewhere classified
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT03714256
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT03714256 through Pure Global AI's free database. This phase not specified trial is sponsored by Permobil, Inc. and is currently Completed. The study focuses on Disability Physical. Target enrollment is 33 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.