Nellcor Bedside Respiratory Patient Monitoring System With Respiration Rate Version 2.0

Medtronic

Status: Completed

Conditions: Monitoring Arterial Oxygen Saturation

Study type: Observational

Funder types: Industry

Identifiers

NCT02075398

COVMOPR0428

Details and patient eligibility

About

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

Enrollment: 35 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 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

Exclusion criteria

• 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).