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Airway Morbidity clinical trials

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NCT ID: NCT05030337 Recruiting - Clinical trials for Mechanical Ventilation Complication

Optimising Ventilation in Preterms With Closed-loop Oxygen Control

Start date: September 5, 2021
Phase: N/A
Study type: Interventional

Many premature infants require respiratory support in the newborn period. Mechanical ventilation although life-saving is linked to complications for the lungs and other organs and its duration should be kept to a minimum. The use of supplemental oxygen may also increase the risk of comorbidities such as retinopathy of prematurity. Therefore, oxygen saturation levels and the amount of inspired oxygen concentration provided should be continuously monitored. Oxygen control can be performed manually or with the use of a computer software incorporated into the ventilator that is called 'closed loop automated oxygen control'(CLAC). The software uses an algorithm that automatically adjusts the amount of inspired oxygen to maintain oxygen saturation levels in a target range. Evidence suggests that CLAC increases the time spent in the desired oxygen target range but there are no data to determine the effect on important clinical outcomes. A previous study has also demonstrated that CLAC reduces the inspired oxygen concentration more rapidly when compared to manual control. That could help infants come off the ventilator sooner. With this study we want to compare the time preterm infants spend on the ventilator when we use the software to automatically monitor their oxygen levels with those infants whose oxygen is adjusted manually by the clinical team. That could help us understand if the use of automated oxygen control reduces the duration of mechanical ventilation and subsequently the complications related to it.

NCT ID: NCT04991545 Recruiting - Covid19 Clinical Trials

Feasibility of the Infra-Red Illumination for Facilitation of Video Scope-tracheal Intubation

Start date: January 13, 2021
Phase: N/A
Study type: Interventional

Airway securing through the placement of an endotracheal tube continues to be the definitive and the global standard management. The successful first attempt is aimed to avoid the consequences of multiple intubation trials as bleeding, tissue swelling, and airway contamination from gastric content that led to considerable morbidity and mortality. Visualization of the larynx and the glottic opening is the key to first-pass success requiring long-term training and availability of specific equipment concerned to that. For confirmation of the position endotracheal tube or its displacement, various clinical and equipment aids to that which are not valid or limited in different scenarios. Video laryngoscopes (VL) have been proposed to improve laryngeal visualization, hence a higher first-pass success rate accomplished. Despite that, there are limitations of video laryngoscope use in different circumstances that requiring adding of other aids to facilitate endotracheal intubation. x

NCT ID: NCT03760679 Recruiting - Airway Morbidity Clinical Trials

Laryngeal Mask Supreme and I-Gel in Edentulate Geriatric Patients

Start date: August 1, 2018
Phase: N/A
Study type: Interventional

The primary aim of this study is to evaluate ease and duration of placing Laryngeal Mask Supreme (LM) and applying I-gel in geriatric patients without teeth. The secondary aim is to compare their effects on ventilation parameters.

NCT ID: NCT03399695 Recruiting - Anesthesia Clinical Trials

Preoxygenation Using High Flow Oxygen : Efficacy and Tolerance in Healthy Volunteers

PreOx-OHD
Start date: January 2, 2018
Phase: N/A
Study type: Interventional

High flow nasal cannula oxygen has been proposed to perform preoxygenation in patients with acute respiratory failure requiring orotracheal intubation in intensive care units. However, its use for preoxygenation before the induction of general anaesthesia in operating room has never been evaluated in term of end tidal oxygen fraction which is the gold standard measurement during preoxygenation before general anaesthesia. The goal of the present study is to measure end tidal oxygen after 3 min of preoxygenation using the recommended method (spontaneous breathing of 100% inhaled oxygen through a face mask) and using high flow nasal canula oxygen, in healthy volunteers.

NCT ID: NCT03251053 Recruiting - Smoking Cessation Clinical Trials

Adverse Airway Effects From Tobacco and E-Cigarettes

Start date: March 28, 2016
Phase: N/A
Study type: Interventional

The purpose of the study conducted at VA Medical Center in Miami is to determine if smoking electronic cigarettes (known as e-cigarettes) that contain nicotine have less negative effects than regular cigarettes on the person's respiratory health. We will assess this by measuring pulmonary function tests, several body molecules and functionality of the airway cells. We will also evaluate how smokers can maintain exclusive electronic cigarettes use. In this study, some people will continue to smoke regular tobacco cigarettes while others will switch to a nicotine-containing electronic cigarette.

NCT ID: NCT02777840 Recruiting - Airway Morbidity Clinical Trials

High Flow Oxygen With THRIVE Gives Better Oxygenation in Rapid Sequence Induction Patients

THRIVE/RSI 1
Start date: March 2015
Phase: N/A
Study type: Interventional

High flow oxygen results in better oxygenation in emergency cases needing rapid sequence induction for anaesthesia. Secondary outcome measure is time for any desaturation.

NCT ID: NCT02104453 Recruiting - Airway Morbidity Clinical Trials

Comparative Evaluation of Three Airway Maneuvers in the Unconscious Apneic Person

Start date: July 2014
Phase: N/A
Study type: Interventional

One-handed E-C clamp mask holding technique, two-handed mask ventilation with jaw thrust, and two-handed mask ventilation with triple airway maneuver are three common airway management maneuvers. Sniffing position may improve ventilation between these three maneuvers. The investigators hypothesize that ventilation efficiency may be different between these three maneuvers whether the patient is in sniffing position or neutral position. The investigators would like to quantify this effect by measuring the expired tidal volume, airway pressure, EtCO2 slope and hemodynamic change between these three maneuvers during anesthesia induction.

NCT ID: NCT02035449 Recruiting - Respiratory Failure Clinical Trials

Video Laryngoscopy in Pre-hospital Critical Care

Start date: December 2013
Phase: N/A
Study type: Observational

Difficult conditions and critically ill and injured patients may complicate endotracheal intubation in the pre-hospital setting. The incidence of complications increase when two or more endotracheal intubation attempts are needed. The aim of this study is to estimate the incidence of difficult pre-hospital endotracheal intubation after the introduction of the McGrath MAC Video laryngoscope as the primary airway device for pre-hospital endotracheal intubation. Hypothesis: • In our pre-hospital critical care teams, staffed with experienced anaesthesiologists, the rate of difficult PHETI (defined as more than one intubation attempt needed to secure a patent airway) is lower than 10 %, when using the McGrath MAC VL as primary choice in pre-hospital intubations.