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Respiratory Insufficiency clinical trials

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NCT ID: NCT01810536 Terminated - Cystic Fibrosis Clinical Trials

High Flow Nasal Oxygen for Children With Cystic Fibrosis Presenting With Respiratory Failure - a Randomized Controlled Study

HIFLOWCF
Start date: April 2013
Phase: N/A
Study type: Interventional

Respiratory exacerbations are frequent among cystic fibrosis patients and supplemental oxygen is usually required. We will compare a new high flow nasal cannula system with Venturi masks for oxygen supplementation to patients with CF hospitalized for respiratory exacerbation.

NCT ID: NCT01810510 Withdrawn - Respiratory Failure Clinical Trials

Impact of PAV Versus NAVA on Patient-Ventilator Synchrony and Respiratory Muscle Unloading

Start date: April 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether two modes of artificial (i.e. mechanical) ventilation have an impact on patient synchrony with the ventilator (breathing machine) and on the patient's work of breathing.

NCT ID: NCT01807663 Terminated - Respiratory Failure Clinical Trials

Validation of a Dynamic Evaluation Tool in Respiratory Failure

TELERESP
Start date: November 2012
Phase: N/A
Study type: Interventional

Determing optimal time of ventilator disconnection is a challenge for both acute and chronic neuromuscular disease. In one case it is helpful for weanning from ventilator and in the other to optimize daytime ventilation in the most severe patients. The investigators propose to validate a new non invasive tool for monitoring respiratroy parameters in neuromuscular patients in both acute and chronic conditions.

NCT ID: NCT01806532 Recruiting - Respiratory Failure Clinical Trials

Regional Lung Inflammation and Expansion in Mechanically Ventilated Patients - a PET/CT Study

Start date: January 2008
Phase: N/A
Study type: Observational

The goal of this study is to investigate acute respiratory distress syndrome (ARDS) and septic lung with positron emission tomography (PET) imaging and to examine the distribution of inflammation, as measured by neutrophil metabolic activity.

NCT ID: NCT01802099 Terminated - Clinical trials for Acute Respiratory Failure

Impact of Early Enteral vs. Parenteral Nutrition on Mortality in Patients Requiring Mechanical Ventilation and Catecholamines

NUTRIREA2
Start date: March 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the hypothesis that, as compared to early intravenous feeding, early nutrition via the enteral route is associated with reduced Day 28-mortality in critically ill patients treated with mechanical ventilation and vasoactive drug.

NCT ID: NCT01797614 Recruiting - Respiratory Failure Clinical Trials

Intra-abdominal Pressures During the Spontaneous Breathing Trial

IAP_SBT
Start date: January 2012
Phase: N/A
Study type: Observational

Increased intra-abdominal pressure (IAP) affects pulmonary dynamics. However, little is studied whether pulmonary dynamics affects IAP. We hypothesize that the change of IAP can also reflect the change of pulmonary dynamics. In this study, we choose patients who received spontaneous breathing trial to answer the hypothesis.

NCT ID: NCT01795196 Withdrawn - Clinical trials for Respiratory Insufficiency

Integrated Pulmonary Index (IPI) as a Determinate of Weaning Success and/or Failure in the Pediatric Population

IPI
Start date: May 2011
Phase:
Study type: Observational

Integrated pulmonary index (IPI) is a tool that monitors respiratory status. It takes into account four parameters: respiratory rate, end-tidal CO2, heart rate and O2 saturation using a pulse oximeter and specialized sidestream CO2 monitor. The device can continuously monitor and display the patient's ventilatory state as a single digit, 1-10. In addition, trends can be kept and it can provide early indication of changes in respiratory status. IPI has only been studied in pediatric patients who are under sedation; however, more uses for the monitoring tool are a possibility. One of those possibilities is to use IPI to monitor pediatric patients during the weaning and extubation process to determine if a specific number, or less than a specific number, is associated with extubation failure. Therefore, clinicians and physicians would be better able to determine if the patient is ready for extubation.

NCT ID: NCT01792258 Recruiting - Heart Failure Clinical Trials

Procedures and Follow-up of Percutaneous Tracheostomy in Intensive Care Unit

Start date: June 2012
Phase: N/A
Study type: Observational

Tracheostomy is worldwide performed in Intensive Care Unit (ICU). According to the current literature, indication for percutaneous tracheostomy (PDT) in ICU are: difficult prolonged weaning, prolonged mechanical ventilation, loss of airway reflex, copious secretions, upper airway obstruction. Many studies have focused on the comparison between different PDT techniques and complication. The aim of our study is to evaluate the procedural features, complications, ICU mortality, quality of life, post-discharge mortality of patients undergoing different PDT techniques performed in ICU.

NCT ID: NCT01788956 Active, not recruiting - Sepsis Clinical Trials

Comparison of Central Venous Oxygen Saturation Measurements by Non-invasive Mespere Venous Oximeter and Central Venous Catheter

Start date: October 2014
Phase: N/A
Study type: Observational

The intent of this study is to validate the venous blood oxygenation measurements of the Mespere VA Oximeter compared to the saturations measured by venous blood sampling through an inserted central vein catheter, which is currently the standard of care for measuring SvO2

NCT ID: NCT01788345 Active, not recruiting - Clinical trials for Acute-on-chronic Respiratory Failure

Prospective Trial of the Bilevel Positive Airway Pressure (by Boussignac) in Emergency Department of Non-invasive Patients Presenting With Acute Hypercapnic Respiratory Failure

Boussignac
Start date: February 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the new Boussignac-system of non-invasive ventilation is as good as the conventional non-invasive System in patients presenting with acute hypercapnic respiratory failure.