Novel Non-Invasive Monitoring Parameter in a Hospital Setting

Completed

Conditions studied: Respiratory Insufficiency, Respiratory Failure

In brief

Data collected from this study will be used to evaluate the performance of a monitoring algorithm.

Key facts

Study ID

NCT01306201

Run by

Medtronic - MITG

People needed

63

Starts

2011-02-01

Expected to finish

2012-03-01

Last updated by the study team

2014-08-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects 18 years old or older
• Written informed consent from the patient or their legally authorized representative before initiation of any study-related procedures
• Subjects on general care floor

You may not qualify if…

• Severe contact allergies to standard adhesive materials
• Abnormalities that may prevent proper application of the device
• Women who are pregnant or lactating
• Subjects with significant arrhythmia

Where it is running

• The University of Colorado Health Sciences Center (UCHSC) — Denver, Colorado, United States
• The Ohio State University Medical Center (OSUMC) — Columbus, Ohio, United States

Full record on ClinicalTrials.gov

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