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Ventilator-Induced Lung Injury clinical trials

View clinical trials related to Ventilator-Induced Lung Injury.

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NCT ID: NCT03435913 Completed - Laparoscopy Clinical Trials

Transpulmonary Driving Pressure and Intra-abdominal Pressure Relationship During Laparoscopic Surgery

Start date: April 19, 2018
Phase: N/A
Study type: Interventional

Objective: The aim of this project is to evaluate how intra-abdominal pressure paired coupled with different ventilatory positive end-expiratory pressure levels affects the transpulmonary driving pressure during pneumoperiteneum insufflation for laparoscopic surgery. Methodology: Patients undergoing laparoscopic surgery will be included. The study will investigate the relationship between intra-abdominal pressure (IAP) and transpulmonary driving pressure (TpDp) and the effect of titration of PEEP on their relationship. At three different levels of intra-abdominal pressure, the respiratory driving pressure (RDp) and TpDp in each subject will be measured in each subject. The same subject will undergo two different ventilation strategies. Demographic data (height, weight, body mass index and sex), ASA physical status (surgical risk classification of the American Society of Anesthesiology), number of previous abdominal surgeries, number of previous pregnancies, and respiratory comorbidities will be collected. Respiratory pressures and mechanics will be recorded at each level of intra-abdominal pressure (IAP) during each ventilatory strategy. The variables recorded will include: airway pressures (Plateau pressure Pplat, Peak pressure, Ppeak), the final esophageal pressure of inspiration and expiration and pulmonary stress index. Mixed linear regression will be used to evaluate the relationship between different PEEP levels, IAP and TpDp by adjusting for known confounders and adding individuals as a random factor. Likewise, an analysis using a mixed linear regression model with the pulmonary stress index as a function of the intra-abdominal pressure, the ventilation regime, and a specific random intercept term for each subject will be performed.

NCT ID: NCT03405779 Recruiting - Clinical trials for Mechanical Ventilation Complication

A New Ultrasonographic Tool to Assess Pulmonary Strain in the ICU

Start date: March 12, 2018
Phase:
Study type: Observational

The primary objective of the study is to create a small dataset of regional pulmonary strain values in patients suffering from pulmonary diseases under mechanical ventilation in an intensive care setting. Hypothesis: The analysis of lung ultrasonographic sequences using speckle-tracking allows the determination of local pleural strain in 4 predetermined pulmonary areas in mechanically ventilated patients suffering from pulmonary diseases.

NCT ID: NCT03401463 Completed - Clinical trials for Respiratory Tract Infections

Assesment of the Endotracheal Tube Cuff Pressure Values in ICU Pateints Before and After Training Seminar

Start date: October 26, 2017
Phase: N/A
Study type: Interventional

There is no accepted standard for the frequency of monitoring endotracheal tube cuff pressures (ETCP). the investigators plan on comparing two strategies for monitoring ETCP in mechanically ventilated patients. Nowadays ETCP is evaluated once every 24 hours. Next, the investigator want to conduct training for medical and nursing staff. After the training, ETCP will be measured every 8 hours. The aim of the study is to prove that more frequent pressure control (3 times a day) reduces the occurrence of abnormal ETCP.

NCT ID: NCT03367221 Recruiting - Clinical trials for Ventilator-Induced Lung Injury

Physiological Response in Lung Transplant Recipients Undergoing Neurally Adjusted Ventilatory Assist

TRANS-NAVA
Start date: November 23, 2017
Phase: N/A
Study type: Interventional

Primary Graft Dysfunction (PGD) respresents the leading cause of mortality in early post-operative period of Lung Tranplantation (LTx). Protective ventilatory strategy could potentially reduce the risk of PGD in these patients. Neurally Adjusted Ventilatory Assist (NAVA) is an assisted ventilation mode that could allow to adopt this strategy. Aim of the study is to assess the feasibility of NAVA in the early post-LTx phase and to describe the breathing pattern and the physiological relationship between neural respiratory drive and different levels of ventilatory assist, in the absence of pulmonary vagal afferent feedback.

NCT ID: NCT03278769 Completed - Clinical trials for Ventilator-Induced Lung Injury

Ventilator Settings on Patients With Acute Brain Injury

Start date: June 1, 2019
Phase: N/A
Study type: Interventional

The present study is an explorative analysis of the relationship between cerebral blood perfusion and oxygenation and lung mechanical variables at different ventilator settings. It is a safety study excluding patients with severe lung injury or brain edema.

NCT ID: NCT03245684 Not yet recruiting - ARDS Clinical Trials

Assisted or Controlled Ventilation in Ards (Ascovent)

ASCOVENT
Start date: September 1, 2017
Phase: N/A
Study type: Interventional

The present pilot randomized controlled clinical trial will test the hypothesis that in patients with ARDS, fixing ventilator settings to the conventional protective ventilatory strategy (VT 6 ml/kg ideal body weight and Pplat ≤ 30 cmH2O, PEEP according the PEEP/FiO2 table), control modes of mechanical ventilation will be associated to a concentration of pulmonary and systemic inflammatory mediators lower than the concentration of inflammatory mediators observed during assisted modes of mechanical ventilation.

NCT ID: NCT03231735 Active, not recruiting - Clinical trials for Bronchopulmonary Dysplasia

Mid and Standard Frequency Ventilation in Infants With Respiratory Distress Syndrome

MIDAS
Start date: August 2, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine, in preterm infants less than 37 weeks gestation with respiratory distress who are ventilated in the first 48 hours after birth, if mid frequency ventilation strategy using ventilator rate of ≥ 60 to ≤ 150 per minute compared with standard frequency ventilation strategy using ventilator rates of ≥ 20 to < 60 per minute will increase the number of alive ventilator-free days after randomization and reduce the risk of ventilator induced lung injury.

NCT ID: NCT03165760 Completed - Clinical trials for Postoperative Complications

Protective Mechanical Ventilation and Risk of Postoperative Complications in Abdominal Surgery

Start date: July 1, 2015
Phase: N/A
Study type: Interventional

Randomized controlled trial, comparing two groups of 40 patients each scheduled for open major abdominal surgery. The intervention group was ventilated with a protective strategy consisting on a low Tidal volume (Vt) (6ml/kg of predicted body weight (PBW)), positive end expiratory pressure (PEEP) = 10 cm H2O and recruitment manoeuvres (RM) after disconnection from the ventilator, the control group had classic ventilation (Vt = 8 ml/kg of PBW, PEEP = 4 cmH2O and no RM).

NCT ID: NCT03140579 Withdrawn - Critical Illness Clinical Trials

Effect of PEEP on Lung Recruitment and Homogeneity Over Time in Moderate to Severe ARDS

APRV
Start date: June 1, 2018
Phase:
Study type: Observational

This study evaluates the effect of airway pressure release ventilation (APRV) on lung homogeneity and recruitment in patients with moderate to severe acute respiratory distress syndrome (ARDS). It will do this by comparing the homogeneity of ventilation and recruitment prior to a patient being ventilated on APRV, and at 30, 60 and 120 minutes after starting APRV.

NCT ID: NCT03135691 Active, not recruiting - Clinical trials for Ventilator-Induced Lung Injury

Intraop Ventilation Management and Postop Pulmonary Complications in High Risk Patients for OSA

Start date: March 18, 2017
Phase:
Study type: Observational

Lung protective ventilation (LPV) has been proposed to reduce the incidence of postoperative pulmonary complications (PPCs), and protect against ventilator induced lung injury (VILI).