Accuracy of Acoustic Rainbow Monitoring (ARM) Sensor

Masimo

Status: Completed

Conditions: Healthy

Treatments: Device: ARM sensor

Study type: Interventional

Funder types: Industry

Identifiers

NCT03124862

TR18351C-TP15637A

Details and patient eligibility

About

The purpose of the study was to conduct a side by side comparison of the accuracy of the respiratory rate (RR) between our Acoustic Rainbow Monitoring (ARM) sensor and the Oridian Microcap Capnograph in healthy adults. Our hypothesis was that the ARM sensor would have comparable or a better performance than the capnograph.

Enrollment: 26 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• healthy adult volunteers

Exclusion criteria

• under age of 18

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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26 participants in 1 patient group

Test group

Experimental group

Description:

The subjects will be enrolled into the test group and will receive ARM sensor.

Treatment:

Device: ARM sensor