Pulse Oximetry- Evaluating Resp Rate- PCBA-1

Completed

Conditions studied: Healthy Subjects

In brief

To assess performance of resp rate parameter in a monitoring system PCBA-1

Key facts

Study ID

NCT01791582

Run by

Medtronic - MITG

People needed

27

Starts

2012-10-01

Expected to finish

2012-10-01

Last updated by the study team

2013-12-06

Who can join

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

You may qualify if…

• Male or female subjects ages 18 or older.
• Subject is willing and able to provide written consent.

You may not qualify if…

• Subject has severe contact allergies that may cause a reaction to standard adhesive materials found in pulse oximetry sensors, ECG electrodes, respiration monitor electrodes or other medical sensors.
• Subjects with abnormalities that may prevent proper application of the device.
• 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 within thirty seconds).
• Women who are pregnant or lactating.

Where it is running

• Covidien — Boulder, Colorado, United States

Full record on ClinicalTrials.gov

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