Accuracy of CardioWatch 287-2 During Profound Hypoxia

Hypoxia Clinical Trial

— ACW2  

Official title:

Accuracy of CardioWatch 287-2 During Profound Hypoxia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05542732
• Other study ID #: CIV-21-12-038447
• Status: Completed
• Phase: N/A
• Start date: June 4, 2022
• Est. completion date: June 27, 2022

Study information

• Verified date: September 2022
• Source: Corsano Health B.V.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In an individual's SpO2 range from 100 to 73 %, this study calibrates and evaluates the accuracy of SpO2 measurement by CW2 in comparison to reference pulse oximeter (Nellcor PM10) or CO-oximetry, Pulse rate (PR) and respiratory rate (RR) were calibrated based on the same Nellcor equipment and the frequency of end-tidal CO2 respectively.

Description:

The study is designed in accordance with Medical electrical equipment - Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment ISO 80601-2-61:2017, Corrected version 2018-02 and ISO 80601-2-55. SpO2: Testing to confirm the accuracy of the SpO2 monitoring according to ISO 80601-2-61 Clause 201.12.1.101 201.12.1.101 RR Testing: Testing to confirm the accuracy of the respiration rate monitoring according to ISO 80601-2-55. Volunteers respirated spontaneously, no efforts were made to include all ranges of respiration during the study. PR Testing: Testing to confirm the accuracy of the PR monitoring according to ISO 80601-2-61 Clause 201.12.1.104. No efforts were made to influence PRs of volunteers. An accelerometer and PPG filters are built in CW2 in order to form the basis to exclude non-eligible test results.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 12
• Est. completion date: June 27, 2022
• Est. primary completion date: June 18, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Healthy non-disabled subjects with American Society of Anesthesiologists health score (ASA) of 1 or 2.

2. The subject is aged =18 and = 65 years.

3. The subject is not intellectual disabled, and has provided informed consent and is willing to comply with the study procedures.

Exclusion Criteria:

1. Heavy smokers or individuals exposed to high levels of carbon monoxide that result in elevated carboxyhemoglobin levels.

2. Individuals subject to conditions that result in elevated levels of methemoglobin

3. Individuals with hypoxia (SpO2 < 95 % at 21 % of oxygen)

4. Severe claustrophobia

5. Subject is known with altitude disease

6. The subject is obese (BMI = 31 kg/m2).

7. The subject has a known history of moderate to severe heart disease, lung disease, kidney or liver disease.

8. The subject is diagnosed with moderate to severe asthma.

9. The subject is known with a hemoglobinopathy or history of anemia, e.g. sickle cell anemia, thalassemia, ... who, in the opinion of the investigator, would make them unsuitable for study participation.

10. The subject has any other serious systemic illness.

11. Any injury, deformity, or abnormality at the sensor sites that in the opinion of the investigators would interfere with the sensors working correctly.

12. The subject has a history of fainting or vasovagal response.

13. The subject has a history of sensitivity or allergy to local anesthetics or disinfectants.

14. The subject has a diagnosis of Raynaud's disease.

15. The subject has unacceptable collateral circulation based on exam by the investigator.

16. The subject is pregnant, lactating or trying to get pregnant.

17. The subject is unable or unwilling to provide informed consent or is unable or unwilling to comply with study procedures.

18. The subject has any other condition, which in the opinion of the investigators would make the subject unsuitable for the study.

19. The subject refuses to remove nail-vanish.

Related Conditions & MeSH terms

• Hypoxia

Intervention

Device:
• CardioWatch 287-2
CardioWatch 287-2 (CW2 Test Device or CW2). This medical device is based on the precursor CardioWatch 287-1 approved by EU-MDR under number 20M00011CRT01, CW2 has two red, two infrared and two green LEDs, and two photosensors compared to its precursor.

Locations

Country	Name	City	State
Belgium	Complementair Medisch Centrum (CMC) Europe	Genk

Sponsors (2)

Lead Sponsor	Collaborator
Corsano Health B.V.	Ziekenhuis Oost-Limburg

Country where clinical trial is conducted

Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pulse Oximetry	SpO2	1 hour
Primary	Pulse rate	Heart rate in beats per minutes	1 hour
Primary	Respiratory rate	In breaths per minutes	1 hour