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Trending of Respiratory Rate Using the Nellcor™ Bedside Respiratory Patient Monitoring System

NCT03593603 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 37

Last updated 2019-05-23

No results posted yet for this study

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.

Conditions

  • Patients Prescribed Non-invasive Respiratory Monitoring

Interventions

DEVICE

Nellcor™ 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 & Collaborators

  • Medtronic - MITG

    lead INDUSTRY

Principal Investigators

  • Paul J Amoroso, MD · MultiCare Institute for Research and Innovation

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-07-11
Primary Completion
2019-05-03
Completion
2019-05-03
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03593603 on ClinicalTrials.gov