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Tracheal Intubation Morbidity clinical trials

View clinical trials related to Tracheal Intubation Morbidity.

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NCT ID: NCT01351259 Completed - Clinical trials for Mechanical Ventilation Complication

Continuous Control of Polyurethane Tracheal-cuff Pressure: Efficiency of a Pneumatic Device

Nosten
Start date: February 2010
Phase: Phase 4
Study type: Interventional

Underinflation and overinflation of tracheal cuff are common in intubated patients, including those intubated with polyurethane-cuffed tubes. The aim of this study is to determine the efficiency of a pneumatic device in controlling cuff pressure.

NCT ID: NCT01289769 Completed - Hypertension Clinical Trials

The Effect of Dexmedetomidine on Hemodynamic Response During Double Lumen Endotracheal Intubation

Start date: March 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effect of dexmedetomidine on hemodynamic responses during laryngoscopy and double lumen endotracheal intubation and assess the adverse effect related to complications of dexmedetomidine.

NCT ID: NCT01215422 Completed - Clinical trials for Tracheal Intubation Morbidity

Success of Pediatric Anesthesiologists in Learning to Use Videolaryngoscopes

Start date: January 2007
Phase: Phase 3
Study type: Observational

There are two new instruments on the market that anesthesiologists use when putting a breathing tube into the lungs of patients. The purpose of this study is to see how easily anesthesiologists can learn to use them in children.

NCT ID: NCT01118533 Completed - Sore Throat Clinical Trials

Impact of Blades Used for Scheduled Orotracheal Intubation on Postoperative Sore Throat

MPLIT
Start date: September 2010
Phase: N/A
Study type: Interventional

Orotracheal intubation following general anesthesia requires blades to be performed. The risk of patients contamination with infectious agents related to reusable metal blades leads to promote single-use blades. Some of these latter are plastic and this material may need more strength to lift the jaw and expose the larynx before orotracheal intubation. Sometimes, change of blade, from plastic to metal, during the procedure is necessary to increase the larynx exposure. This change of blade may increase the frequency of sore throat following orotracheal intubation. Consequently, the study hypothesis is an increase of both sore throat intensity and frequency with the plastic blades compared with the metal blades. The primary purpose of the present study is to compare the impact of these two types of blades, metal versus plastic, on sore throat intensity and frequency following scheduled orotracheal intubation for general anesthesia

NCT ID: NCT01116999 Completed - Clinical trials for Tracheal Intubation Morbidity

Retrograde Light Target Tracheal Intubation Technique:Clinical Comparison With Direct Pharyngoscopic Tracheal Intubation

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

The investigators hypothesise that, for novices, light guided tracheal intubation will improve the time and success rate of this clinical skill compared to standard direct tracheal intubation.