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Clinical Trials/NCT04562584
NCT04562584
Completed
Not Applicable

Accuracy of Pulse Oximeters With Profound Hypoxia

MyHomeDoc Ltd.1 site in 1 country12 target enrollmentJune 3, 2020
ConditionsOximetry

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Oximetry
Sponsor
MyHomeDoc Ltd.
Enrollment
12
Locations
1
Primary Endpoint
Saturation level measurement
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The aim of this project is to test the accuracy of pulse oximeters (devices intended to measure oxygen saturation in blood noninvasively) during mild, moderate and severe hypoxia (a lower-than-normal concentration of oxygen in arterial blood); ie, a range of arterial HbO2 saturations from 100 to down to 70%. This is done by comparing the reading of the pulse oximeter during brief, steady state hypoxia with a gold-standard measurement of blood oxyhemoglobin (hemoglobin carrying oxygen) saturation, that is arterial blood sample processed in a laboratory.

Registry
clinicaltrials.gov
Start Date
June 3, 2020
End Date
June 4, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
MyHomeDoc Ltd.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • The subject is male or female, aged ≥18 and \<
  • The subject is in good general health with no evidence of any medical problems.
  • The subject is fluent in both written and spoken English.
  • The subject has provided informed consent and is willing to comply with the study procedures.

Exclusion Criteria

  • The subject is obese (BMI\>30).
  • The subject has a known history of heart disease, lung disease, kidney or liver disease.
  • Diagnosis of asthma, sleep apnea, or use of CPAP.
  • Subject has diabetes.
  • Subject has a clotting disorder.
  • The subject a hemoglobinopathy or history of anemia, per subject report or the first blood sample, that in the opinion of the investigator, would make them unsuitable for study participation.
  • The subject has any other serious systemic illness.
  • The subject is a current smoker.
  • Any injury, deformity, or abnormality at the sensor sites that in the opinion of the investigators' would interfere with the sensors working correctly.
  • The subject has a history of fainting or vasovagal response.

Outcomes

Primary Outcomes

Saturation level measurement

Time Frame: 1 hour

Induction of hypoxia by having subjects breathe mixtures of nitrogen, room air, and carbon dioxide to allow measurement of oxyhemoglobin saturation between 70-100%. Each plateau level of oxyhemoglobin saturation was maintained for at least 30 seconds or until reference pulse oximeters readings were stable

Study Sites (1)

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