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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: 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: 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: NCT00778219 Completed - Clinical trials for Intubation, Endotracheal

Comparison of Heart Rate Variability Among Tracheal Intubation Methods

Start date: October 2008
Phase: N/A
Study type: Observational

60 patients, in three group of 20 patients each, scheduled for surgery needing general anesthesia will be researched. Group A: tracheal intubation of single lumen tube using laryngoscope. Group B: single lumen tube using lightwand. Group C: double lumen endobronchial cath. During general anesthesia, the spectral power of heart rate variability at three periods: (1) preoperation baseline (2) pre-intubation and (3) post-intubation will be calculated and compared to investigate the autonomic stimulation effect of different tracheal intubation methods.

NCT ID: NCT00434720 Completed - Clinical trials for Intubation, Endotracheal

Comparison of GlideScope Specific Stylet to Malleable Stylet for GlideScope Intubation

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

The GlideScope video laryngoscope (Verathon) is an intubating device that uses a high-resolution camera embedded into a plastic laryngoscope blade. An LED provides illumination. The GlideScope often provides a good laryngoscopic view, but passing the endotracheal tube (ETT) through the vocal cords is sometimes difficult. Because of the 60 degree anterior curvature of the GlideScope's blade, ETT's must have stylets inserted so that the ETT distal tip can be positioned anteriorly. Various authors have recommended different angles of the ETT to optimally place it into the trachea. Previous study demonstrated that 90 degree sharp bend was both faster and subjectively easier in a heterogeneous group of intubators. With the introduction of a rigid GlideScope Specific Stylet by the manufacturer, the question arises as to the the best configuration of stylet for the ETT. Therefore, this prospective, randomized, single-blinded trial is proposed. The null hypothesis is that there will be no difference between the GlideScope Specific Stylet and the standard malleable stylet.

NCT ID: NCT00378651 Completed - Clinical trials for Intubation, Endotracheal

Use of the Stethoscope to Confirm Breathing Tube Placement

Start date: September 2006
Phase: N/A
Study type: Interventional

This study is intended to validate the use of neck auscultation with an electronic stethoscope during intubation to confirm tracheal tube placement. It is hypothesized that the ability to confirm correct tube placement with this technique will be similar to that of the end-tidal CO2 monitor, the current gold-standard device for confirming tracheal intubation.

NCT ID: NCT00349245 Completed - Clinical trials for Intubation, Endotracheal

Dexmedetomidine vs. Remifentanil for Sedation During AFI

Start date: June 2006
Phase: Phase 4
Study type: Interventional

The objective of this study is to determine the efficacy and safety of Dexmedetomidine, a selective alpha-2 adrenoceptor agonist, which has recently gained increased popularity for ICU and intraoperative sedation as a sedative during awake fiberoptic intubation, as compared to Remifentanil. The hypothesis is that Dexmedetomidine will provide at least equal if not better conditions (sedation and analgesia) required for awake fiberoptic intubation (Ramsay Sedation Scale 3) with less respiratory and cardiovascular adverse effects, as well as less recall than Remifentanil.