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Mechanical Ventilation clinical trials

View clinical trials related to Mechanical Ventilation.

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NCT ID: NCT03115840 Active, not recruiting - Sepsis Clinical Trials

Measuring Outcomes of Activity in Intensive Care

MOSAIC
Start date: March 27, 2017
Phase:
Study type: Observational

Millions of older adults are hospitalized for a critical illness each year and although they are more likely than ever to survive this illness, they commonly face significant morbidity in the form of disabilities in basic self-care activities and in mobility in the months and years afterwards. A better understanding of the underlying risk factors for disability following critical illness is greatly needed, including the effect that activity during hospitalization may have on these outcomes. Therefore, we designed the Measuring OutcomeS of Activity in Intensive Care (MOSAIC) observational study to evaluate the relationship between activity (measured more rigorously than in prior investigations) and disability, physical function, and cognitive function in survivors of critical illness 3 and 12 months after ICU discharge.

NCT ID: NCT03097692 Completed - Clinical trials for Mechanical Ventilation

Does Preconditioning Affects Other Organs in Patients Undergoing Open Heart Surgery ?

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

An association between white blood cell count (WBC), neutrophil-lymphocyte ratio , and inflammatory process is well known . Ischemic preconditioning reduces the inflammation

NCT ID: NCT03096106 Completed - Clinical trials for Mechanical Ventilation

Visual Assessment for Pressure-time Curve

Start date: December 1, 2016
Phase: N/A
Study type: Observational

Airway pressure-time (P-t) curve and stress index (SI) assessment have been proposed to guide the mechanical ventilation settings and minimize ventilator-induced lung injury.

NCT ID: NCT03078517 Completed - Clinical trials for Mechanical Ventilation

Comparison of the LMA Protector and the I-gel

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

Investigators aim to compare two supraglottic airway devices; the i-gel and the newly developed laryngeal mask airway protector in terms of airway sealing effect, the insertion success rate, and the incidence of complications in anesthetized patients.

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: NCT03066388 Terminated - Clinical trials for Mechanical Ventilation

Accuracy of Pulse Pressure Variations Measured by a Non Invasive Digital Device to Predict Fluid Responsiveness

Start date: April 2012
Phase: N/A
Study type: Interventional

It has been well established that only 40 to 60% of the patients hospitalized for inflammatory response syndrome (SIRS) positively respond to volume expansion (VE). The fluid responsiveness is usually estimated by assessing VE-induced change in stroke volume (SV). To guide prescriptions and possibly avoid deleterious effects of inappropriate VE, several clinical studies demonstrated that invasive dynamic indices based on heart-lung interactions permit an accurate prediction of the hemodynamic effects induced by VE. Mechanical ventilation induces cyclic changes in intrathoracic and transpulmonary pressures that transiently affect venous return, right and left ventricular preload, resulting in pronounced cyclic changes in SV in preload-dependent, but not in preload-independent patients. These cyclic changes in SV can be evaluated by the cyclic changes in arterial pulse pressure. Several studies have shown that pulse pressure variation is able to predict fluid responsiveness in patients in the operating room and intensive care unit (ICU). However, this technique requires percutaneous arterial catheterization, which is associated with several rare but serious complications (thrombosis, infections, pseudoaneurysm,hematoma, and bleeding). A method for assessing noninvasive arterial blood pressure using an electropneumatic control loop was introduced by Penaz in 1973. Briefly, the blood volume in a finger is measured and kept constant by applying corresponding external pressure. The continuously changing external pressure needed to keep the volume constant directly corresponds to the arterial pressure and, therefore can be used as continuous measurement of arterial blood pressure. Numerous studies evaluating the accuracy of this technology, e.g., Finapres™ (Ohmeda Monitoring Systems, Englewood, CO), and more recently of the Infinity CNAP™ SmartPod (Dräger Medical AG & Co.KG, Lübeck, Germany). The basic operating principle of the CNAP™ is similar to the Finapres™, but CNAP™ uses multiple control loops. It has recently been shown that CNAP provides real-time estimates of mean arterial blood pressure (MAP) comparable with those measured by an invasive intraarterial catheter system during general anaesthesia. The accuracy of the measures and the respiratory variations in pulse pressure obtained with the CNAP system have not yet been studied in ICU.

NCT ID: NCT03031860 Completed - Clinical trials for Mechanical Ventilation

Semi-quantitative Cough Strength Score (SCSS)

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

Cough strength score will give true prediction of Extubation outcome

NCT ID: NCT03030911 Completed - Clinical trials for Mechanical Ventilation

Dexmedetomidine vs Midazolam on Resting Energy Expenditure in Critically Ill Patients

Start date: January 1, 2017
Phase: Phase 4
Study type: Interventional

The aim of this study is to compare the effect of dexmedetomidine on resting energy expenditure in relation to the midazolam in critically ill patients using indirect calorimetry

NCT ID: NCT02989415 Completed - Clinical trials for Mechanical Ventilation

Assessment of Ventilatory Management During General Anesthesia for Robotic Surgery

AVATaR
Start date: August 3, 2017
Phase:
Study type: Observational

The aim of this study is to assess the incidence of postoperative pulmonary complications in patients undergoing mechanical ventilation during general anesthesia for robotic surgery, to characterize current practices of mechanical ventilation and to evaluate a possible association between ventilatory parameters and postoperative pulmonary complications.

NCT ID: NCT02976844 Completed - Clinical trials for Mechanical Ventilation

Effect of Positive End-expiratory Pressure on Optimal Balloon Volume During Esophageal Pressure Monitoring

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

Esophageal pressure (PES), which has been used as a surrogate for pleural pressure. The volume of esophageal balloon can influence the accuracy of monitoring esophageal pressure. The optimal balloon volume is directly dependent on surrounding pressure. In the present study,the investigators will observe the optimal volume of esophageal balloon during the different PEEP in bench and clinical study.