Sensor Off Study Using a Nellcor USB Pulse Oximetry Monitor Interface Cable

Completed · Not applicable

Conditions studied: Healthy Volunteers

In brief

The purpose of this study is to validate that the device posts a Sensor-Off message within the time frame stated in the proposed claims.

Key facts

Study ID

NCT02265783

Run by

Medtronic - MITG

People needed

20

Starts

2014-09-01

Expected to finish

2014-11-01

Last updated by the study team

2017-05-01

Who can join

Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Male or female subjects 18 or older (inclusive)
• Subject is able to participate for the duration of the study
• Subject is willing to sign an informed consent

You may not qualify if…

• Previous injury or trauma to fingers or hands that may change blood flow or vascular supply and affect our ability to test sensors
• Physiologic abnormalities that prevent proper application of pulse oximetry sensor
• Severe contact allergies that cause a reaction to standard adhesive materials such as those found in medical sensors and electrodes

Where it is running

• Boulder Clinical Laboratory — Boulder, Colorado, United States

Full record on ClinicalTrials.gov

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