Nellcor Bedside Respiratory Patient Monitoring System With Respiration Rate Version 2.0

Completed

Conditions studied: Monitoring Arterial Oxygen Saturation

In brief

To validate the Respiration Rate Version 2.0 algorithm, housed in the Nellcor Bedside Respiratory Patient Monitoring System, for performance during motion conditions.

Key facts

Study ID

NCT02075398

Run by

Medtronic - MITG

People needed

35

Starts

2013-12-01

Expected to finish

2013-12-01

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…

• Subject with abnormalities that may prevent proper application of the devices
• Physiologic abnormalities that prevent proper application of pulse oximetry sensor
• Severe contact allergies that cause a reaction to standard adhesive materials such as those fund in medical sensors and electrodes
• Subjects with significant arrhythmia, as determined by subject self-report during screening and I/E criteria assessment at study start. (Three events of irregularities in radial pulse with thirty seconds).

Where it is running

• Boulder Clinical Laboratory — Boulder, Colorado, United States

Full record on ClinicalTrials.gov

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