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Usability Validation of Patient Monitoring Device for Pressure Injury Prevention and Fall Detection

NCT03121144 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 34

Last updated 2020-06-01

Study results available
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Summary

This study describes a procedure to collect a subject's position, movement, physiological data and usability information using Masimo's investigational device.

Conditions

  • Pressure Ulcer
  • Pressure Injury
  • Falls Injury

Interventions

DEVICE

Masimo Centroid System

Noninvasive positional monitoring device

Sponsors & Collaborators

  • Masimo Corporation

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-03-01
Primary Completion
2019-03-27
Completion
2019-03-27
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 NCT03121144 on ClinicalTrials.gov