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Intubation, Endotracheal clinical trials

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NCT ID: NCT05143606 Completed - Clinical trials for Intubation, Endotracheal

3D Printed Model Simulator or Virtual Reality Software for Training Fiberoptic Intubation Skill

Start date: January 15, 2022
Phase: N/A
Study type: Interventional

Fiberoptic-assisted intubation is an advanced skill that requires learners' practice as well as clinical experience during the anesthesiology residency training period. Current training methods including airway simulators and virtual reality software are used by medical schools worldwide. The objective of this study is to compare the learner's fiberoptic intubation performance between training with a 3D-printed simulator and a virtual reality software.

NCT ID: NCT02293226 Not yet recruiting - Cardiac Arrest Clinical Trials

Video-laryngoscopy During Chest Compression

VIDEO
Start date: November 2014
Phase: N/A
Study type: Interventional

The investigators will compare the success rates and time to successful intubation of endotracheal intubation during simulated pediatric and infant resuscitation with and without chest compression using four different video-laryngoscopes.

NCT ID: NCT02291653 Completed - Cardiac Arrest Clinical Trials

Pediatric Endotracheal Intubation

EMS
Start date: November 2014
Phase: N/A
Study type: Interventional

We hypothesized that the McGrath MAC EMS is beneficial for intubation of pediatric manikins while performing CPR. In the current study, we compared effectiveness of the McGrath MAC EMS and MIL laryngoscopes in child resuscitation with and without CC.

NCT ID: NCT02291640 Recruiting - Cardiac Arrest Clinical Trials

Pediatric Intubation Among Nursing

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

The aim of this study was to compare time, success rates of video laryngoscope and direct laryngoscope for the emergency intubation with an immobilized cervical spine in a standardized pediatric manikin model.

NCT ID: NCT02291627 Recruiting - Trauma Clinical Trials

Pediatric Intubation With Difficult Airway

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

The aim of this study was to compare time, success rates of different video laryngoscopes for the emergency intubation with an immobilized cervical spine in a standardized pediatric manikin model.

NCT ID: NCT01865643 Completed - Anesthesia, General Clinical Trials

A Comparison of Two GlideScope Intubation Techniques

Start date: May 2013
Phase: N/A
Study type: Interventional

The aim of this study is to compare the hemodynamic response to tracheal intubations using the standard technique versus the alternative GS intubation technique. As secondary outcomes the investigators will analyze procedure time, success rate and injury rate. The investigators hypothesize that the alternative intubation technique will have a shorter procedure time and lower injury rate when compared to the standard technique of GS intubation.

NCT ID: NCT01156233 Completed - Clinical trials for Intubation, Endotracheal

Tube Tip Position in Orally Intubated 0-4year Old Children: Assessment of the Precision of Two Clinical Techniques

Start date: May 2010
Phase: N/A
Study type: Interventional

In pediatric anesthesia it is very important to place the endotracheal tube into the right position. This study compares two clinical location methods. The hypothesis means that the two techniques have the same precision of the location of the tip position of a cuffed MICROCUFF (Kimberly-Clark)endotracheal tube.

NCT ID: NCT00968058 Completed - Clinical trials for Intubation, Endotracheal

Leak Pressure of Uncuffed Pediatric Endotracheal Tubes

Start date: June 2009
Phase: N/A
Study type: Observational

Children and adults frequently need a 'breathing tube' when having anesthesia for surgery. The breathing tube is usually inserted after the anesthesia doctor puts a patient to sleep with medicine, so they do not feel the breathing tube. In children, there is often a leak of air between the tube and the windpipe, as the tube is not an exact fit. Anesthesia doctors usually listen for this leak around the tube by listening to the chest with a stethoscope while gently filling the lungs with oxygen from the anesthesia machine. The leak tells them if the tube is the correct size, or too small, or too tight. If it is too small, or too tight, they usually change the tube for a better fit. The purpose of this study is to see what happens to this leak in the 30 minutes after the tube is placed. No one really knows if the leak gets bigger, smaller, or stays the same. Knowing what happens to the leak will help anesthesia doctors to decide whether to change the breathing tube or not. This is important, as a tube that is too tight can lead to breathing difficulty after removing the tube at the end of surgery, and a tube that is too small may make it difficult for the breathing machine to work effectively for the patient as a result of a large leak of air or oxygen.

NCT ID: NCT00917033 Completed - Obesity Clinical Trials

Tracheal Intubation of Morbidly Obese Patients. GlideScope Versus Direct Laryngoscopy

Start date: September 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to examine whether orotracheal intubation in morbidly obese patients is faster, gentler and safer using the GlideScope videolaryngoscope than with the Macintosh direct laryngoscope.

NCT ID: NCT00912990 Terminated - Clinical trials for Intubation,Endotracheal

Pediatric Elective Intubation With and Without Muscle Relaxation Utilizing the Shikani Optical Stylet

Start date: January 2007
Phase: N/A
Study type: Interventional

The investigators' primary specific aims are to demonstrate that: 1. Pediatric patients with normal airways, undergoing elective surgical procedures, can be successfully intubated when deeply sedated, without the use of muscle relaxants using the Shikani Optical Stylet. 2. Shikani intubation of pediatric patients is equally effective in children that are deeply sedated or paralyzed as evidenced by a non-significant difference in: - Time to intubation (defined as no more than a 30 second time difference between the two groups); - Incidence of adverse events.