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ARDS clinical trials

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NCT ID: NCT03371680 Completed - ARDS Clinical Trials

Kinetics of Surfactant Proteins, Phosphatidylcholine and Body Water in Intensive Care Unit (ICU)

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

Analysis of kinetics of phosphatidylcholine and specific surfactant proteins, total body water and water turnover in patients with acute respiratory distress syndrome (ARDS) and in intensive care unit (ICU) patients by using non radioactive isotopes as deuterium and Carbon-13.

NCT ID: NCT03237806 Completed - ARDS Clinical Trials

Effects of Sedation on Transpulmonary Pressure and Lung Homogenous

ARDS
Start date: May 31, 2015
Phase: N/A
Study type: Interventional

The acute respiratory distress syndrome (ARDS) is characterized by severe respiratory failure. Open Lung and Lung Protective Strategy have been proved to improve mortality of ARDS patients. Preserving spontaneous breathing (SB) is good for inflating the lung lobe near diaphram during mechanical ventilation, however, strong respiratory drive could generate more transpulmonary pressure in ARDS patients, which increase the stress and strain in injured lung. Nonetheless, it's not clear if sedative has any effects on transpulmonary pressure of ARDS patients.The purpose of this study is to investigate the effects of sedation on transpulmonary pressure of ARDS patients.

NCT ID: NCT03225807 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Implementation of Lung Protective Ventilation in Patients With Acute Respiratory Failure

IMPROVENT
Start date: March 2016
Phase:
Study type: Observational

This is a quality improvement study with the purpose of observing and measuring the effects of implementation of a proven standardized lung protective ventilation protocol in the new electronic medical record system iCentra across all Intermountain Healthcare hospitals. Approximately 14,000 records will be accessed for this study from a database of mechanically ventilated patients established for quality improvement purposes. The investigators hypothesize that implementation of a standardized computerized lung protective ventilation protocol across all Intermountain Healthcare hospitals will be feasible, will decrease initial tidal volumes to the target 6 ml/kg PBW, and will improve outcomes. The objectives of this study are to: - Determine if the implementation of lung protective ventilation (with a 6 ml/kg PBW tidal volume ventilation protocol on initiation of mechanical ventilation) improves outcomes in patients with acute respiratory failure requiring mechanical ventilation - Determine if the implementation of lung protective ventilation (with a 6 ml/kg PBW tidal volume ventilation protocol on initiation of mechanical ventilation) improves outcomes in the sub-group of patients with the acute respiratory distress syndrome (ARDS) - Measure compliance with the implementation of a computerized lung protective ventilation protocol at 12 Intermountain Healthcare hospitals

NCT ID: NCT03200314 Completed - ARDS Clinical Trials

Blood Recirculation and vvECMO

Start date: August 13, 2017
Phase:
Study type: Observational

A prospective, observational study will be performed measuring recirculation of blood through a veno-venous Extracoporeal Membrane Oxygenation (vvECMO) in patients with acute respiratory distress syndrome (ARDS) on vvECMO. ECMO blood flow will be adjusted with respect to recirculation.

NCT ID: NCT03076983 Completed - Clinical trials for Mechanical Ventilation

Assessment of the Capability of PulmoVista 500 to Continuously Monitor Changes of Ventilation Over Time

Start date: May 30, 2017
Phase:
Study type: Observational

The results of this study will help to define the capability and reliability of PulmoVista 500 to detect changes in both global and regional ventilation.

NCT ID: NCT02871063 Completed - ARDS Clinical Trials

Effect of Altitude on the Evolution of Acute Respiratory Distress Syndrome

Start date: August 1, 2016
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this piece of research is to assess the effect of altitude on the clinical evolution of ARDS. For this purpose, patients who live and receive care at sea level are compared with those who live and receive care at high altitudes. For reasons of convenience, a cut-point of 1500 meters above sea level was chosen. In addition to this, it will be sought to assess whether adjusting the cut-points for the severity categories of ARDS improves the ability to predict some adverse events, by comparison with unadjusted cut-points. The results of this research will probably be disruptive, and will provide the first information yet about the effect of altitude on ARDS; they will therefore be of great interest for the international scientific community and for the direct care of patients. A high bibliometric impact is to be expected.

NCT ID: NCT02703012 Completed - ARDS Clinical Trials

Clinical Application of Electrical Impedance Tomography for Individual Adjustment of Ventilator Settings

CLEAR
Start date: January 2016
Phase: N/A
Study type: Interventional

First clinical application of an algorithm for individual adjustment of ventilator settings using electrical impedance tomography.

NCT ID: NCT02644798 Completed - ARDS Clinical Trials

Nucleotide Polymorphism in ARDS Outcome

Start date: January 1, 2016
Phase:
Study type: Observational

Acute respiratory distress syndrome (ARDS) is characterized by increased pulmonary vascular permeability and reduced aerated lung tissue. With an extremely high hospital mortality among 35 - 46%, current therapeutic strategies to increase ARDS survival are still limited. Advances in etiology and pathology of ARDS are urging. Numerous genetic variants were identified associated with ARDS outcome. By whole-exome sequencing association study, our goal was to explore the associations between genetic variants and ARDS outcome.

NCT ID: NCT02638844 Completed - ARDS Clinical Trials

Assessment of Right Ventricular 2d-strain in Acute Respiratory Distress Syndrome

ARDStrain
Start date: December 2015
Phase: N/A
Study type: Observational

Assessment of right ventricular (RV) function in patients with acute respiratory syndrome (ARDS) is warranted because RV failure is frequent and associated with worse outcome. Transthoracic echocardiography is the cornerstone of RV assessment but it remains challenging. Quantification of RV deformation by speckle-tracking imaging echocardiography (STE) is a widely available and reproducible technique that readily provides an integrated analysis of all segments of the RV. This study aims to investigate the accuracy of STE-derived strain parameters in assessing RV function during ARDS.

NCT ID: NCT02595060 Completed - ARDS Clinical Trials

Granulocyte Macrophage-Colony Stimulating Factor (GM-CSF) Inhalation to Improve Host Defense and Pulmonary Barrier Restoration

GI-HOPE
Start date: June 1, 2016
Phase: Phase 2
Study type: Interventional

This trial evaluates efficacy and safety of inhaled molgramostim (rhGM-CSF) in 45 patients with pneumonia associated acute respiratory distress syndrome (ARDS). A third of the patients will receive 150 mcg inhaled molgramostim, another third 450 mcg and the remaining third will receive inhaled placebo for 3 days. The patients will be followed for 28 days.