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Patient Monitoring clinical trials

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NCT ID: NCT04959136 Not yet recruiting - Patient Monitoring Clinical Trials

Feasibility Study Of Ambulatory Monitoring System

Start date: September 1, 2021
Phase: N/A
Study type: Interventional

This is a clinical, data collection study conducted at one site. This study will collect open comments, user feedback and parameter raw data to support patient monitoring product development. Subjects participating in this study will be monitored with the site's standard of care primary monitor and the investigational device as the secondary monitor while enrolled in this study. No subject care decisions or diagnoses will be made based on information obtained from the investigational secondary monitor.

NCT ID: NCT04481308 Recruiting - Patient Monitoring Clinical Trials

Non-invasive Carbon Dioxide Monitoring and Endoscopic Retrograde Cholangiopancreatography Patients

Start date: October 2022
Phase:
Study type: Observational

CO2 monitoring through non-invasive methods to provide an early warning of hypoventilation during procedural sedation.

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: NCT03764709 Not yet recruiting - Patient Monitoring Clinical Trials

Continuous Wireless Monitoring in Internal Medicine Unit: the Green Line From Hospital to Territory

GreenLightHT
Start date: January 27, 2019
Phase: N/A
Study type: Interventional

Study Information Indication* This is a prospective, randomized, controlled, open-label, monocentric study for the evaluation of two different settings of critically ill patients recovered in Internal Medicine unit (IMU) and subsequently sent to subacute managed care unit or to earlier discharge, in order to evaluate the effectiveness of a wireless monitoring of clinical conditions vs. a traditional clinical monitoring on outcomes (critical adverse events, clinical exacerbations). Phase*: 4, observational prospective Number of subjects*: GROUP A and GROUP B: N=300 patients (150 per arm)

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: NCT03039738 Terminated - Patient Monitoring Clinical Trials

Surveillance Monitoring as an Alternative to Telemetry

Start date: April 3, 2017
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the impact of surveillance monitoring versus telemetry monitoring on clinical, healthcare economics, resource utilization, and qualitative outcomes.

NCT ID: NCT02962570 Active, not recruiting - Patient Monitoring Clinical Trials

On-Demand Oxygen Delivery System Study

Start date: November 2016
Phase: N/A
Study type: Interventional

The main goal of this study is to determine if supplemental oxygen given only when the patient is inspiring (demand delivery) is more effective than constant-flow oxygen given during all phases of the breath regardless if the patient is breathing it in. A previous study in volunteers (NCT02886312) showed that the oxygen saturation in the blood and the concentration of oxygen breathed out from the lungs (end-tidal oxygen) was higher when given in demand (inhalation only) mode. A secondary goal is to determine in patients, whether turning oxygen delivery off during expiration improves the accuracy of end-tidal CO2 (Carbon Dioxide) monitoring. This was found to be the case in the previous volunteer study. The investigators want to determine if these improvements are also observable in relatively healthy patients undergoing procedural sedation and analgesia. The efficacy of the demand mode will be determined by measuring the resulting difference in oxygen saturation and end-tidal oxygen levels. The investigators will alternate between traditional oxygen delivery (continuous flow) and demand delivery (flow only during inhalation) for two minutes in each mode after which oxygen saturation and end-tidal oxygen will be measured. End-tidal CO2 measurement will be compared with those during the brief time when O2 flow is stopped.

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