Fingertip Pulse Oximeter Clinical Test

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01605955

Enrollment

Registered

2012-05-25

Start date

2011-11-30

Completion date

2011-12-31

Last updated

2012-05-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

SPO2

Keywords

SPO2

Brief summary

The purpose of this study is to validate the SpO2 accuracy of pulse oximeter equipment in comparison to gold-standard measurements of blood SaO2 by a CO-oximeter

Interventions

None listed

Study design

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

25 Years to 32 Years

Healthy volunteers

Yes

Inclusion criteria

* Subjects participate in the study on a voluntary basis * All subjects should be in good health at the time of the study. Unless specified otherwise in the protocol, the following values could be applied: COHb\<3 %, MetHb\<2 %, ctHb\>10 g/dl; * Inclusion criteria should serve the purpose of the study

Exclusion criteria

* Smokers or individuals exposed to high levels of carbon monoxide that result in elevated carboxyhaemoglobin levels, unless specific dyshaemoglobins are called for in the study protocol. * Individuals subject to conditions that result in elevated levels of methaemoglobin, unless specific dyshaemoglobins are called for in the study protocol. * Subjects who would be placed at undue medical risk associated with any procedures called for in the protocol (e.g. arterial cannulation or hypoxia). * Age: young person and that of more than 50 years old.

Outcome results