Bedside Respiratory Patient Monitoring System - Sensor Off Study

Completed

Conditions studied: Healthy Volunteers

In brief

Use of an investigational oximetry system to evaluate the triggering of the "sensor off" status with the marketed off-the-shelf sensors.

Key facts

Study ID

NCT02075346

Run by

Medtronic - MITG

People needed

18

Starts

2013-11-01

Expected to finish

2013-11-01

Last updated by the study team

2014-03-03

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Male or female subjects 18 years 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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