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Respiratory Insufficiency clinical trials

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NCT ID: NCT03697863 Enrolling by invitation - Clinical trials for Acute Respiratory Failure

Noninvasive NAVA Versus Flow-triggered Noninvasive Pressure Support in Pediatric Respiratory Failure

Start date: October 3, 2018
Phase:
Study type: Observational

Acute Hypoxemic Respiratory Failure (AHRF) is a leading cause of admission in Pediatric Intensive Care Unit (PICU). Traditional treatment includes endotracheal intubation and mechanical ventilation, that are invasive and not free from risks. Recent experiences from pediatric studies showed that Non-Invasive Pressure Support Ventilation (NIV-PS) has been associated with lower intubation rate, adverse events and mortality compared to mechanical ventilation delivered by an endotracheal tube. Nonetheless, in pediatric ARF, the application of a well-synchronized NIV-PS is technically challenging due to the presence of leaks and the age-specific characteristics of pediatric respiratory pattern (high respiratory rate, short inspiratory/expiratory time and weak inspiratory effort). Consequently, NIV-PS often results in difficult patient-ventilator interaction, with a failure rate up to 43% . Neurally Adjusted Ventilatory Assist (NAVA) is a new form of ventilatory assistance wherein the ventilator applies positive pressure throughout inspiration synchronously and proportionally to the Electrical Diaphragm activity (Edi). Thus, NAVA is not influenced by large leaks around uncuffed endotracheal tubes or noninvasive interfaces. Studies in intubated children found that NAVA improved interaction by reducing asynchronies and optimizing ventilator cycling.Two recent studies showed that the application of Non-Invasive NAVA (NIV-NAVA) in children with ARF is feasible and may reduce asynchronies as compared to NIV-PS. More recently, in a recent RCT of our group, we demonstrated that NIV NAVA in children was associated with lower asynchronies, longer synchronization time between patient and ventilator at lower peak and mean airway pressure. However no data are published to address the question if the better synchronization between patients and ventilator obtained with NIV NAVA could lead to a reduction in intubation rate and PICU outcomes. To address this question, we designed an observational retrospective study aiming to define if early delivered NIV NAVA could reduce intubation rate if compared with traditionally flow-cycled NIV PS in hypoxemic children admitted to PICU.

NCT ID: NCT02687074 Enrolling by invitation - Respiratory Failure Clinical Trials

Effects of HFNC on Moderate and Severe Respiratory Failure Patients

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

Respiratory failure is the danger for the patients admitted in ICU, mechanical ventilation could save a lot of patients' life, however, it prolongs patients' ICU stay and hospital stay. High flow nasal cannula (HFNC) has advantages of PEEP effects, reducing dead space, increasing EELV and improving comfort, and it has been used to treat respiratory failure patients. In recent study, HFNC could improve mortality of respiratory failure patients with P/F<200mmHg in the subgroup. The investigators want to start a randomized controlled study to evaluate the effects of HFNC on the patients with respiratory failure.

NCT ID: NCT02523872 Enrolling by invitation - Clinical trials for Respiratory Insufficiency

Description of Fluid Balance in Patients With Acute Respiratory Failure

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

The specific aim of this study is to gather data on fluid balance, intravenous medication administration, electrolyte balance, and diuretic and dialysis use in patients with acute respiratory failure who might benefit from a strategy designed to limit fluid administration.

NCT ID: NCT02290236 Enrolling by invitation - Clinical trials for Sleep Apnea, Obstructive

Monitored Saturation Post-ICU

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

The overall aim with this project is to describe the correlation between measured and charted saturation after intensive care and also describe the saturation-pattern in these patients. The investigators will also correlate post-ICU desaturations measured as oxygen denaturation index and complications to pre-ICU obstructive sleep apnea and the STOP BANG screening questionnaire.

NCT ID: NCT02204215 Enrolling by invitation - Sepsis Clinical Trials

Electric Acupuncture for ICU-acquired Weakness in Mechanical Ventilation Patients

EA-ICUAW
Start date: January 2014
Phase: N/A
Study type: Interventional

Intensive care unit acquired weakness (ICU-AW) is common and dramatically affect recovery. The purpose of this study is to determine whether electric acupuncture therapy is effective in the treatment of ICU-AW especially in the patients receiving mechanical ventilation with sepsis or multiorgan system failure.

NCT ID: NCT01966861 Enrolling by invitation - Clinical trials for Acute Respiratory Failure

Weaning From Mechanical Ventilation Guided by Lung Ultrasound (Brazilian WEANLUS)

WEANLUS-BR
Start date: March 2016
Phase: Phase 3
Study type: Interventional

The present study aims to evaluate the impact of a weaning strategy based on identification of early signs of respiratory distress by lung ultrasound and the consequent implementation of a "clinical optimization" protocol as compared to usual care.

NCT ID: NCT01569217 Enrolling by invitation - Respiratory Failure Clinical Trials

Regional Distribution of Ventilation to Assess Respiratory Muscle Dysfunction

DREM
Start date: June 2011
Phase: N/A
Study type: Observational

The aim of this study is to better discriminate respiratory muscle dysfunction by comparing the measurements of thoracoabdominal motion obtained by an optoelectronic recording and the conventional tests of respiratory muscle strength. The final objective is to better select in the future the patients who need more specific assessment of diaphragmatic function like "maximal transdiaphragmatic pressure" measurement and "phrenic nerve stimulation".