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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04811300
Other study ID # mCVI003
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 9, 2021
Est. completion date May 15, 2021

Study information

Verified date May 2021
Source Intelomed, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Description:

In this prospective clinical study the mCVI® device is a mobile application used to simply verify the algorithm when the mobile video reads a patients pulse rate and respiratory rate while spontaneously breathing. There is no facial recognition technology. There is no immediate feedback given to the research team to act upon or provide for further clinical care decisions. In real time, the mCVI® device will be compared to two commercially-available Masimo pulse oximeter devices in a single visit.


Recruitment information / eligibility

Status Completed
Enrollment 9
Est. completion date May 15, 2021
Est. primary completion date April 11, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 70 Years
Eligibility Inclusion Criteria: - Healthy adults between the ages of 21 - 70 - Informed consent obtained and signed Exclusion Criteria: - 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
There is no intervention
There is no intervention

Locations

Country Name City State
United States Scitech Campus Corporation Columbus Ohio

Sponsors (1)

Lead Sponsor Collaborator
Intelomed, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pulse Rate Verification in Different Lighting Conditions To demonstrate that in 4 different lighting environments common to home and office/clinical conditions, mCVI® accurately captures pulse rate in comparison to Masimo pulse oximeter devices. 2 months
Primary Respiration Rate Verification in Different Lighting Conditions To demonstrate that in 4 different lighting environments common to home and office/clinical conditions, mCVI® accurately captures respiratory rate in comparison to Masimo pulse oximeter devices. 2 months
Secondary Skin Tone Pulse Rate Verification in Different Lighting Conditions To demonstrate that in 4 different lighting environments common to home and office/clinical conditions, mCVI® accurately captures pulse rate in healthy volunteers with a variety of skin tones using the Fitzpatrick Skin Type Scale. 2 months
Secondary Skin Tone Respiratory Rate Verification in Different Lighting Conditions To demonstrate that in 4 different lighting environments common to home and office/clinical conditions, mCVI® accurately captures respiration rates in healthy volunteers with a variety of skin tones using the Fitzpatrick Skin Type Scale. 2 months
See also
  Status Clinical Trial Phase
Completed NCT04297644 - mCVI Pilot Study: Algorithm Verification
Completed NCT04692064 - mCVI Confirmatory Clinical Study: Algorithm Verification
Withdrawn NCT05233319 - mCVI Confirmatory Clinical Study: Algorithm Verification With Healthy Volunteers