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Patient Monitoring clinical trials

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NCT ID: NCT04472208 Completed - Patient Monitoring Clinical Trials

AMS Evaluation Study

Start date: February 26, 2021
Phase: N/A
Study type: Interventional

A study to evaluate the operational and functional features of the Ambulatory Monitor Solution (AMS) as well as the ease of use of the system.

NCT ID: NCT03574272 Completed - Patient Monitoring Clinical Trials

Patient Transfer Monitoring System in Hospital Using Mobile IoT Technology

Start date: May 16, 2018
Phase: N/A
Study type: Interventional

This trial is multi-center prospective study to develop Patient Transfer Monitoring system using mobile lot network and the Risk Factor Detection System and apply to real In-Hospital Patients and verify the efficacy.

NCT ID: NCT02886312 Completed - Patient Comfort Clinical Trials

Evaluation of Oxygen Delivery Through Nasal Cannula in Volunteers

Start date: August 2015
Phase: N/A
Study type: Interventional

This study will evaluate patient comfort and oxygen delivery efficiency when providing supplemental oxygen through a nasal cannula to volunteers using an instrumented oxygen delivery system. The goals of the study are to evaluate different oxygen flow rates and oxygen delivery modes. In addition, the investigators will investigate if the system can detect apnea (cessation of breathing) and removal of the nasal cannula. The investigators will also investigate how well high flow oxygen delivered only during inspiration is tolerated and how much the end-tidal oxygen increases after two minutes of high oxygen flow delivered only during the inhalation phase of the breath.

NCT ID: NCT02571465 Completed - Hemodynamics Clinical Trials

Assessment of Fluid Responsiveness in Patients After Cardiac Surgery

POP
Start date: April 2015
Phase: N/A
Study type: Observational

To overcome the limited accuracy of functional hemodynamic parameters such as stroke volume and pulse pressure variation (SVV and PPV) during spontaneous breathing, a Passive Leg Raising (PLR) manoeuvre has been suggested as a reliable predictor of fluid responsiveness. Aim of this study was to evaluate fluid responsiveness using SVV, PPV and PLR during the transition from controlled to spontaneous breathing in cardiac surgery patients