Patients Prescribed Non-invasive Respiratory Monitoring
Conditions
Brief summary
This is an open-label, non-randomized, prospective, descriptive study of the Nellcor™ Bedside Respiratory Patient Monitoring System using the Nellcor™ Respiration Rate parameter and Nellcor™ Adult Respiratory Sensor The study is intended to gain further information in the clinical space on the function of the Nellcor™ Respiration Rate parameter. The primary objective is to describe spot check (e.g. manual observation) of respiration rate versus cumulative automated counting (trend) of respiratory rate as measured using the Nellcor™ Bedside Respiratory Patient Monitoring System with the Nellcor™ Respiration Rate parameter.
Interventions
DEVICENellcor™ Bedside Respiratory Monitoring System
Nellcor™ Bedside Respiratory Patient Monitoring System with Nellcor™ Respiration Rate Software and the Nellcor™ Adult Respiratory Sensor to provide continuous respiration rate monitoring
Sponsors
Medtronic - MITG
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. 18 years or older. 2. A patient who meets the weight requirement for the sensor (e.g. \>30kg). 3. A patient at the study site on a General Care Floor (surgical or medical/non-surgical to be distributed equally) and prescribed standard vital sign checks. 4. Patient is willing and able to provide written informed consent.
Exclusion criteria
1. Expected length of stay is \< 4 hours. 2. Patient is pregnant or lactating. 3. Patient 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. 4. Patient has an abnormality that may prevent proper application of the device. 5. Patient is in atrial fibrillation. 6. Patient has a documented history of frequent premature atrial contractions (PACs) or premature ventricular contractions (PVCs), defined as greater than 3 in 30 seconds or greater than 6 in 60 seconds within the past 3 months. 7. Patient has an implanted pacemaker. 8. Patient has excessive nail polish that cannot be removed or other dye or discoloration of the finger. 9. Patient has diagnosed central apnea or diagnosed significant obstructive sleep apnea. 10. Patient is currently using continuous positive airway pressure (CPAP). 11. Patient is unwilling or unable to sign informed consent. 12. Evidence that the patient cannot understand the purpose and risks of the study and would require a legally authorized representative to sign informed consent. 13. Patient is participating in another potentially confounding clinical study. 14. Extreme motion conditions such as patient is prescribed to walk more than once per hour or is prescribed a medical device resulting in constant movement.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Agreement of RR measured by spot checks vs continuous monitoring | at least 4 hours | Bias and a range of agreement of the differences between RR measured by spot checks and RR measured using the Nellcor™ Bedside Respiratory Patient Monitoring System |
Countries
United States
Outcome results
None listed