Algorithm Verification Clinical Trial
Official title:
A Single-Center, Prospective Clinical Study to Demonstrate That in 4 Different Lighting Conditions mCVI® Accurately Captures Pulse Rate and Respiratory Rate in 10 Healthy Volunteers in Comparison to a Commercially-Available Masimo Pulse Oximeter Device
| 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 |
| Verified date | May 2021 |
| Source | Intelomed, Inc. |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
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.
| 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 |
| Country | Name | City | State |
|---|---|---|---|
| United States | Scitech Campus Corporation | Columbus | Ohio |
| Lead Sponsor | Collaborator |
|---|---|
| Intelomed, Inc. |
United States,
| 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 |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
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