Status:
COMPLETED
Pulse Oximetry- Evaluating Resp Rate- PCBA-1
Lead Sponsor:
Medtronic - MITG
Conditions:
Healthy Subjects
Eligibility:
All Genders
18-50 years
Brief Summary
To assess performance of resp rate parameter in a monitoring system PCBA-1
Eligibility Criteria
Inclusion
- Male or female subjects ages 18 or older.
- Subject is willing and able to provide written consent.
Exclusion
- 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.
Key Trial Info
Start Date :
October 1 2012
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
October 1 2012
Estimated Enrollment :
27 Patients enrolled
Trial Details
Trial ID
NCT01791582
Start Date
October 1 2012
End Date
October 1 2012
Last Update
December 6 2013
Active Locations (1)
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1
Covidien
Boulder, Colorado, United States, 80301