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Mechanical Ventilation clinical trials

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NCT ID: NCT03185962 Completed - Clinical trials for Mechanical Ventilation

Predictors Of Successful Extubation in Critically Ill Patients: Multicentre Observational Study

POSE
Start date: May 1, 2017
Phase:
Study type: Observational

Extubation failure can directly worsen patient outcomes. Therefore, the decision to extubate is a critical moment during an intensive care unit (ICU) stay. The decision to extubate is usually made after a weaning readiness test involving spontaneous breathing on a T-piece or low levels of ventilatory assistance. However, extubation failure still occurs in 10 to 20% of patients. The investigators focused on previously reported physiological risk factors, and were able to obtain from common clinical practice: 1) age, 2) underlying cardiovascular disease, 3) underlying respiratory disease or occurrence of pneumonia, 4) rapid shallow breathing index (RSBI), 5) positive fluid balance during the previous 24 hours, 6) the ratio of arterial oxygen partial pressure to fractional inspired oxygen, 7) Glasgow Coma Scale, 8) respiratory tract secretions. The investigators aimed to assess the incidence and risk factors for extubation failure among critically ill patients who passed the 30 min spontaneous breathing test (SBT) using a low level of pressure support (PS) with positive end-expiratory pressure (PEEP), in a prospective multicenter study.

NCT ID: NCT03155555 Completed - Clinical trials for Mechanical Ventilation

Comparison of Carotid Peak Systolic Velocity Variation With Aortic Peak Systolic Velocity Variation in Pediatric Non-Cardiac Surgery

Start date: December 2016
Phase:
Study type: Observational

The purpose of this study is to evaluate whether carotid Doppler peak systolic velocity can be an easy to measure possible surrogate for echocardiographic measurement of aortic peak systolic velocity variation which is an index of fluid responsiveness in mechanically ventilated children intra-operatively.

NCT ID: NCT03138148 Completed - Clinical trials for Mechanical Ventilation

Evaluation of the Patient-ventilator Asynchrony During Mechanical Ventilation for Pediatric Acute Respiratory Failure

Asynchrony
Start date: May 26, 2010
Phase: N/A
Study type: Observational

The synchronization between the patient and the ventilator is an essential objective during mechanical ventilation (MV). Maintaining the patient's respiratory activity during MV reduces ventilation pressures, improves oxygenation, and decreases sedation. In order to do this, the inspiratory or expiratory effort of the patient must be detected by the respirator' sensor systems, so that the assistance delivered by the respirator is coordinated with the patient's respiratory cycles. The usual systems do not actually detect the beginning of the effort but its result: variation in flow rate or pressure at the respirator circuit, which depends on the patient's respiratory mechanics and sensitivity of the sensor. This detection is currently imperfect, which generates asynchrony between the patient's needs and the assistance of the respirator. The asynchrony comprises the periods of delay between the beginning of the inspiration (or expiration) and the response of the respirator, but also of the unsuitable cycles: inspiratory efforts of the patient not detected by the respirator, or inversely triggering assistance in the absence of inspiration by the patient (self-initiation), or delivery of 2 cycles of assistance for a single inspiration (double triggering). Asynchrony is a risk factor for prolonged mechanical ventilation in adults. Adult studies have shown that patient-ventilator asynchrony is common during MV, and is associated with prolonged MV duration. An association with length of stay in intensive care and in hospital was also observed. In children, patient-ventilator synchronization is more difficult to achieve than in adults due to a higher respiratory rate and smaller current volumes. The impact of patient-ventilator asynchrony on evolution has not been studied in pediatrics. Patient-ventilator synchronization could be improved by the development of new ventilatory modes. The new NAVA (neurally adjusted ventilatory assist) ventilation mode detects the patient's breathing efforts earlier by monitoring the electrical activity of the diaphragm through the esophagus. This new mode seems to improve synchronization in children. NAVA ventilation may therefore be a step forward, but its clinical benefits remain to be seen. The objective of this study is to evaluate the impact of patient-ventilator asynchrony on the duration of mechanical ventilation in children with acute respiratory failure.

NCT ID: NCT03118804 Completed - Clinical trials for Mechanical Ventilation

Weaning From Mechanical Ventilation Guide by Assessment of Lung Tidal Distribution With EIT

Start date: October 18, 2016
Phase:
Study type: Observational

To evaluate whether EELI, RVD, GI were good predictor for weaning from mechanical ventilation

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: 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