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ChroniSense Polso Wrist Worn Respiration Rate Validation Study

NCT03750344 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2019-02-05

No results posted yet for this study

Summary

20 volunteer test subjects will be entered into an accuracy study that is designed to validate accuracy of the respiratory rate of the Polso Monitoring system

Conditions

  • Respiratory Rate

Interventions

DEVICE

Diagnostic test

Comparison of respiratory rates in normal subjects as observational with end tidal CO2. No treatment or interventions will be performed

Sponsors & Collaborators

  • ChroniSense Medical Ltd.

    lead INDUSTRY

Principal Investigators

  • Arthur D Cabrera, MD · Avista Adventist Hospital

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-11-06
Primary Completion
2018-11-09
Completion
2018-11-30
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 NCT03750344 on ClinicalTrials.gov