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Active clinical trials for "Respiratory Distress Syndrome"

Results 1361-1370 of 1388

Comparison of Two Methods to Estimate the Lung Recruitment

Acute Respiratory Distress SyndromeAcute Lung Injury

In this study the investigators aim to compare two common methods to estimate the lung recruitment in ALI/ARDS patients.

Unknown status2 enrollment criteria

Discovery of New Early Detection Biomarkers of Acute Respiratory Distress Syndrome

Acute Respiratory Distress Syndrome

The goal of this project is to find a series novel biomarkers by differential proteomic techniques that can improve the early diagnosis and develop a more efficient therapy to enhance ARDS patient survival rate.

Unknown status5 enrollment criteria

Respiratory Mechanics Registry for ARDS Patients

Acute Respiratory Distress Syndrome

This registry was proposed to investigate the epidemiology of respiratory mechanics in patients with ARDS through collecting data from a QI project which was constituted with systematic assessments of respiratory mechanics and gas exchange.

Unknown status3 enrollment criteria

EVLWI Exhibits Pulmonary and Systemic Permeability in Sepsis Related ALI/ARDS

Sepsis Related Acute Lung Injury/Acute Respiratory Distress Syndrome

To investigate the possible mechanisms of pulmonary and systemic permeability change including cytokine, extravascular lung water index (EVLWI), and oxygenation parameters in patients with sepsis related acute lung injury (ALI)/acute respiratory distress syndrome (ARDS).

Unknown status7 enrollment criteria

NIV NAVA Versus NIV-PS in Pediatric Patients - Pilot Study

Acute Respiratory Failure

This pilot study will be an observational no randomize study in which the NiNAVAped protocol will be applied solely to the NIV NAVA arm.

Unknown status25 enrollment criteria

Breathing Pattern, WOB and Gas Exchange in Patients With Acute Respiratory Distress Syndrome During...

Work of BreathingARDS1 more

There is little evidence about the mechanical characteristics and muscular function in patients with Acute Respiratory Distress Syndrome (ARDS) at the time of weaning of the mechanical ventilation, as well as the behavior of the mechanical properties, breathing pattern, muscular effort, and gas exchange during a successful and failed spontaneous breathing trial.

Unknown status9 enrollment criteria

Cerebral and Renal Oximetry Study in Preterm Patients Who Require Surfactant Administration

Respiratory Distress Syndrome of Prematurity

Respiratory distress syndrome of prematurity (RDSP) is an acute respiratory condition that occurs in preterm infants due to pulmonary surfactant deficiency. Exogenous surfactant administration is a crucial therapeutic measure in the management of RDSP, being the 'less invasive surfactant administration technique' (LISA) the gold standard, according to the latest reviews. Oximetry based on near-infrared spectroscopy is a non-invasive monitoring modality that provides continuous information on the degree of regional hemoglobin saturation present in the underlying tissue, mainly in the venous compartment. It is thus, a reflection of the balance between oxygen supply and demand of oxygen to the tissues. We intend to perform a prospective analysis of newborns under 32 weeks of gestational age who require surfactant administration, as we wish to study cerebral and renal perfusion by oximetry in the group of patients who receive surfactant by LISA and in the group of patients who receive surfactant via endotracheal tube (patients intubated at birth for stabilization), since there are few data published in the literature. Our main hypothesis is that the administration of surfactant by LISA technique does not negatively influence cerebral and renal oximetry. Our secondary hypothesis is that patients requiring intubation at birth will present greater hemodynamic and respiratory instability in the first 72 hours of life, with a greater decrease in cerebral and renal oximetry with the administration of surfactant, compared to the group that does not require intubation at birth.

Unknown status3 enrollment criteria

The ECOVITA Study - Validation of LUS Score in SARS-CoV-2 Disease, i.e COVID-19

Respiratory Distress Syndrome

Lung Ultrasound (LUS) has been revealing an extremely useful tool to identify and monitor complications from Sars-COV-2 disease. Recently, a research group has proposed a score, named LUS Score, able to optimize the use of this diagnostic technique. LUS Score is computed analyzing chest posterior and lateral spaces, considering the number of artefacts generated by the inflammed interstitium (B lines), the characteristics of the pleural line and the presence or not of consolidation areas. The comparison between LUS and chest tomography (CT), the current gold standard for the diagnosis of interstitial pneumonia by COVID-19, has confirmed from the preliminary data, the reliability of such technique. Hence, the validation on a really large sample size of the ultrasound tool performed by dedicated personnel with high expertise, may allow the validation both in the clinical practice and in emergency and ordinary wards.

Unknown status7 enrollment criteria

The Critical Care Response to the COVID-19 Pandemic in Madrid

COVID-19ARDS1 more

Description of the adaptation of ICUs in the region of Madrid to que surge in demand of critical care due to COVID-19

Unknown status2 enrollment criteria

Effect of Corticosteroid Treatment on Prognosis in ARDS Secondary to Covid-19

Acute Respiratory Distress Syndrome Secondary to Covid-19

Study conducted on hospitalized patient in critical ill units in Nancy and Metz to evaluate if early corticosteroid treatment in first seven days after admission improve patients outcome in Acute Respiratory Distress Syndrome secondary to Covid-19 compared to later corticosteroid therapy or no treatment. Also comparison of acquired infection with or without corticosteroid treatment during hospitalisation.

Unknown status5 enrollment criteria

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