Clinical Trials Logo

ARDS clinical trials

View clinical trials related to ARDS.

Filter by:

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: NCT02958748 Not yet recruiting - ARDS Clinical Trials

Change of Immune Cell of ARDS Patients:an Observational Study

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

To evaluate change of different immune cellsduring ARDS and its impact on prognosis.

NCT ID: NCT02945917 Recruiting - ARDS Clinical Trials

Positive End-expiratory Pressure and Esophageal Catheter Optimal Calibration Volume in ARDS Patients

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

The use of esophageal balloon catheter to estimate pleural pressure has gained renewed popularity in recent years. Indeed, measurement of transpulmonary pressure may allow a more pathophysiological-based approach to ventilator strategy in acute respiratory distress syndrome (ARDS) patients. Nevertheless, it is well known that esophageal balloon catheter derived parameters can be influenced by several patient-related or technical-related factors. During a PEEP trial, the investigators will observe in-vivo the esophageal pressure and derived measurements obtained using different esophageal balloon calibration volumes.

NCT ID: NCT02902055 Suspended - ARDS Clinical Trials

Paediatric Ards Neuromuscular Blockade Study

PAN
Start date: December 1, 2019
Phase: Phase 4
Study type: Interventional

Paediatric acute respiratory distress syndrome (ARDS) is a manifestation of severe, life-threatening lung injury. Care for paediatric patient is mainly supportive and based on what works in adults and personal experiences, including the use of mechanical ventilation. However, differences in lung physiology and immunology between (young) children and adults suggests that adaptation of adult practices into paediatrics may not be justified. A study in adults with severe ARDS showed that early use of neuromuscular blocking agents (NMBA) improved 90-day survival and increased time off the ventilator without increasing muscle weakness. It is unknown if this is also true for paediatric ARDS

NCT ID: NCT02885675 Recruiting - ARDS Clinical Trials

An Observational Study of the Correlation Between miRNA in Peripheral Blood and Prognosis in Patients With ARDS

Start date: March 2016
Phase: N/A
Study type: Observational

To evaluate the correlation between the value of miRNA related to ARDS and vascular endothelial cell and ARDS severity, vascular endothelial cell damaging degree,mortality in patients with ARDS.

NCT ID: NCT02885584 Active, not recruiting - ARDS Clinical Trials

Conventional Mechanical Ventilation and High Frequency Percussive Ventilation: Comparison of Their Effects on Alveolar Recruitment and Distension by CT-scan in Early ARDS Patients

Start date: December 2013
Phase: N/A
Study type: Interventional

High frequency percussive ventilation (HFPV) is a high frequency ventilation mode in which high frequency pulses accumulate to generate a low frequency tidal volume at a controlled airway pressure. Previous studies have suggested a protective effect of HFPV on lung injury. The goal of our study is to compare, in early ARDS patients, the effects of conventional mechanical ventilation and of high frequency percussive ventilation on alveolar recruitment and distension evaluated by CT-scan

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.