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Mechanical Ventilation clinical trials

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NCT ID: NCT03314701 Recruiting - Clinical trials for Mechanical Ventilation

Mechanical Ventilation in Multiple Fracture Ribs

Start date: October 25, 2017
Phase: N/A
Study type: Interventional

Chest trauma is the most common injury in the emergency trauma and rib fractures is the most common trauma in chest trauma. Severe rib fractures can cause paradoxical respiration and mediastinal swing, which has large effects on respiratory and circulatory system, result in acute respiratory distress syndrome. Mechanical ventilation can significantly improve the hypoxemia of the patients, correct paradoxical respiration, and treat the pulmonary atelectasis

NCT ID: NCT03261440 Recruiting - Clinical trials for Mechanical Ventilation

Cardiac, Pulmonary and Diaphragm Sonography for the Early Diagnosis of the Different Etiologies Underlying Failure of Weaning From Mechanical Ventilation

WEAN US
Start date: November 2016
Phase: N/A
Study type: Observational

Weaning patients off ventilation in an ICU is sometimes difficult, because of three major inter-related etiologies: impaired lung, heart and diaphragm function. In this context, ultrasonography during tests to wean patients off ventilation could make it possible to diagnose cardiac dysfunction, a loss of pulmonary aeration or diaphragm dysfunction and thus reduce the number of failures at extubation. The study will be carried out in 100 patients on mechanical ventilation following abdominal or heart surgery, who will have echocardiography, and pulmonary and diaphragm ultrasonography.

NCT ID: NCT03150264 Recruiting - Clinical trials for Mechanical Ventilation

Prospective Clinical Study of PCV and PCV-VG in Patients Undergoing Bariatric Surgery

Start date: January 16, 2017
Phase: N/A
Study type: Interventional

This study compares the two mechanical ventilation strategies in obese patients undergoing bariatric surgery: pressure-controlled ventilation(PCV) and pressure-controlled ventilation volume-guaranteed(PCV-VG). This is a randomized controlled trial with a sample size of 100 patients whose body mass index(BMI) is over 30kg/m².

NCT ID: NCT02900300 Recruiting - Clinical trials for Mechanical Ventilation

A Biobank for Diaphragm Muscular Fiber

BOTAN
Start date: February 18, 2022
Phase:
Study type: Observational

This non-interventional study focuses on mechanical ventilation used in intensive care unit to supplement ventilatory function in patients. Mechanical ventilation can "paradoxically" be at the origin of complications that can be life-threatening in patients. This muscular pathology is called ventilation-induced diaphragmatic dysfunction (DDIV). Diaphragmatic muscle collected during a digestive surgery for a benign or malignant tumor of the liver requiring surgical excision in contact with the diaphragm from the care will be conserved. The diaphragm biopsy from the care will be retained for biobanking to obtain myoblast in culture which will differentiate in Diaphragm fiber. Then these fibers will be submitted under mechanical stress condition similar to those imposed in vivo by mechanical ventilation to validate in human a model in vitro of diaphragm dysfunction induced by mechanical ventilation. Then the second part of the study will be to evaluate with this model, the efficiency of an antioxidant therapy.

NCT ID: NCT02514655 Recruiting - Clinical trials for Mechanical Ventilation

Simple Mechanical Device to Control Pressure in the Balloon of the Endotracheal Tube to Prevent Ventilator-acquired Pneumonia

PAV-PROTECT
Start date: August 15, 2015
Phase: N/A
Study type: Interventional

Hypothesis: Nosten® device is able to reduce the time of underinflated balloon and removes excess pressure. This device may thus reduce the risk of ventilator-acquired pneumonia (VAP) and early tracheal lesions resulting from intubation with decreased discomfort, morbidity, and nursing workload. The main objective of the investigators is to show that Nosten® device is more effective than monitoring and manual inflation of the balloon of the tracheal tube to prevent VAP occurrence.

NCT ID: NCT02487927 Recruiting - Clinical trials for Mechanical Ventilation

The Classification of Difficult Weaning and the Predictive Value of Relative Factors for Difficult Weaning

Start date: June 2012
Phase: N/A
Study type: Observational

To evaluate the distribution of different types of difficult weaning and the predictive value of weaning relative factors.

NCT ID: NCT02426320 Recruiting - Clinical trials for Mechanical Ventilation

Pilot Study for Sedation Interruption in Children

Start date: April 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to estimate the hypothesized benefit of sedation interruption protocol on mechanical ventilation duration and PICU length of stay. The study will evaluate recruitment rates, and adherence rates of such protocol.

NCT ID: NCT01547507 Recruiting - Clinical trials for Mechanical Ventilation

Performance Evaluation of AirWay Medix Closed Suction System Compared With a Standard Closed Suction System

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

The aim of this prospective, randomized study is to compare the performance, safety, and ease of use (usability) between two closed suction systems, the AirWay Medix Closed Suction System and Kimberly KimVent while intubated with an endotracheal in hospitals and ICU. 26 adults with an endotracheal tube and mechanical ventilation will be randomized into 2 groups to receive one of the following closed suction systems endotracheal tubes: 1. AirWay Medix Closed Suction System 2. KimVent Turbo-Cleaning Closed Suction System Kimberly clarK The groups will be compared regarding the safety, performance and ease of use (usability).

NCT ID: NCT01280019 Recruiting - Cardiac Surgery Clinical Trials

FRC Guided Therapy in Acute Respiratory Failure

Start date: October 2010
Phase: Phase 4
Study type: Interventional

In ventilated patients with acute respiratory failure endotracheal suctioning may lead to alveolar derecruitment, which can be monitored by means of functional residual capacity (FRC) measurements. Regional distribution of ventilation can be followed at bedside using electrical impedance tomography. The investigators hypothesize that a FRC guided recruitment strategy, aimed at restoring a baseline FRC value after open endotracheal suctioning, improves oxygenation and regional distribution of ventilation. In addition the investigators research the impact of such a strategy on the inflammatory response to mechanical ventilation.

NCT ID: NCT01104896 Recruiting - Smoking Clinical Trials

Effect of Daily Nicotine Patch Application on Mechanical Ventilation Weaning in Smoking Patients

NICOREA
Start date: January 2010
Phase: Phase 4
Study type: Interventional

Nicotine patches are frequently used in smoking patients during their stay in the ICU in order to avoid tobacco's weaning symptoms which are likely to interfere with mechanical ventilation weaning. Until now the effectiveness of this treatment has not been proven. The aim of this study (NICOREA study) is to determine if a difference exists on the duration of mechanical ventilation once patients receive or not a nicotine substitute.