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COMPLETEDNANCT03121144

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

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

Lead sponsor: Masimo Corporation•1 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Masimo Corporation

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•1. At least 18 years of age
•2. ICU patient
•3. Primarily bedbound subjects
•4. Able to be monitored for a minimum of approximately 8 hours

Exclusion Criteria

•1. Pregnancy
•2. Prisoner status
•3. Pressure injury stage 2, 3, or ungroupable
•4. Has a pacemaker or internal defibrillator
•5. Has a history of complications with a similar study
•6. Has any medical condition which in the judgment of the Investigator, renders them inappropriate for participation in this study

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: June 1, 2020Terms

Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment34

Start dateMar 2017

Last updatedJun 1, 2020

Condition

Pressure Ulcer Pressure Injury Falls Injury

Locations shown

Baylor University Medical Center

Dallas, Texas

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: June 1, 2020Data synced to Clareo: May 3, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions