Novel Non-Invasive Monitoring Parameter in a Hospital Setting

Medtronic

Status: Completed

Conditions: Respiratory Failure; Respiratory Insufficiency

Study type: Observational

Funder types: Industry

Identifiers

NCT01306201

COVMOPR0131

Details and patient eligibility

About

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

Full description

The goal of this study is to assess equivalency, performance, and accuracy of a new monitoring algorithm in a hospital setting.

Enrollment: 63 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

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

Trial design

63 participants in 1 patient group

In-patient Volunteers

Description:

In-patients from the hospital who choose to participate in the study