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Masimo Centroid System for Pressure Ulcers

N/A
Waitlist Available
Research Sponsored by Masimo Corporation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up at least 8 hours
Awards & highlights
No Placebo-Only Group

Summary

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

Eligible Conditions
  • Fall Injury
  • Bed sore
  • Pressure Ulcers
  • Pressure Sore

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~at least 8 hours
This trial's timeline: 3 weeks for screening, Varies for treatment, and at least 8 hours for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Usability Validation of Masimo Centroid System

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Masimo Centroid SystemExperimental Treatment1 Intervention
Single-arm study. All subjects are enrolled into the test group wherein the noninvasive positional monitoring device will be administered.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Masimo Centroid System
2017
N/A
~40

Find a Location

Who is running the clinical trial?

Masimo CorporationLead Sponsor
116 Previous Clinical Trials
13,533 Total Patients Enrolled
~4 spots leftby Nov 2025
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