mCVI® Lighting Conditions Clinical Study

Completed

Conditions studied: Algorithm Verification

In brief

This single center prospective clinical study is to verify the algorithm of mCVI® in 4 different lighting conditions to accurately capture pulse rate and respiratory rate in 10 healthy subjects in comparison to commercially-available Masimo pulse oximeter devices. This is a non significant risk device.

Key facts

Study ID

NCT04811300

Run by

Intelomed, Inc.

People needed

9

Starts

2021-04-09

Expected to finish

2021-05-15

Last updated by the study team

2021-05-19

Who can join

Age: 21 and older, up to 70. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Healthy adults between the ages of 21 - 70
• Informed consent obtained and signed

You may not qualify if…

• Self-reported medical conditions that could compromise a participant's ability to provide for all breathing samples, pedal the Cubii Pro elliptical, or follow instructions
• Self-reported medical history of respiratory or cardiovascular disease
• Excessive facial hair, facial deformities, or obstructions (like glasses or face masks/shields) that could compromise the recording of pulse rate and respiratory rate of the mCVI®
• Any face lotions or make up foundations that could compromise the recording of pulse rate and respiration rate of the mCVI®
• Missing digits or fingers on one or more hand that would prevent proper recording of Masimo pulse oximeter devices
• Participants wearing nail polish, acrylic nails, or rings on the ring finger of either hand that would prevent the proper use of Masimo pulse oximeter device
• Inability to provide informed consent

Where it is running

• Scitech Campus Corporation — Columbus, Ohio, United States

Full record on ClinicalTrials.gov

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