LIFEGUARD Study - Continuous Respiratory Monitoring on the General Ward

Status Terminated

Clinical Trial Summary

The purpose of this study is to document how often and how severe are the breathing difficulties that patients suffer, while recovering on a general ward following a serious operation

Clinical Trial Description

This is a prospective, 2-center, 2-phase pilot study of post-surgical adult patients on the hospital ward at high risk of developing respiratory and cardiovascular events. Phase I, 70 patients will be 1:1 randomly allocated to Capnostream 20p monitoring system or to PM1000N-RR pulse oximeter monitoring system and the alarms of both devices will be silenced and the screen information blinded, to establish a baseline for the incidence of respiratory events. Phase II, 140 patients will be 1:1 randomly allocated to Capnostream 20p or to PM1000N-RR monitoring but the screen information will be visible at the bedside and through the Vital Sync™ remote patient monitoring system. ;

Study Design

Related Conditions & MeSH terms

Respiratory Complication

Clinical Trial Details

NCT number	NCT03571646
Study type	Interventional
Source	Medtronic - MITG
Contact
Status	Terminated
Phase	N/A
Start date	May 9, 2019
Completion date	December 14, 2019

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