Pulse Oximeter Test | Clinical Trial

Key information

Conditions

Hypoxia Pathological Conditions, Signs and Symptoms Signs and Symptoms Signs and Symptoms, Respiratory

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Observational

Primary location

UCSF Hypoxia Lab

San Francisco, California, 94143, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Good general health with no evidence of medical problems

Exclusion criteria

Smoking
Anemia

Treatment and study plan

Spry Loop oximeter

Device

Oximetry was performed on the subjects and accuracy was determined based on comparison with blood gas analysis.

Primary outcomes

Oximetry Accuracy

Time frame: 30 minutes

RMSE of pulse oximeter

Sponsors and collaborators

Lead sponsor

Spry Health

Industry

Collaborators

University of California, San Francisco

Registry information

Official study title

Accuracy of Pulse Oximeters With Profound Hypoxia

Important dates

Study start: 2017
Primary completion: 2017
Study completion: 2017
First posted: Jun 26, 2018
Registry last updated: Jun 26, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed