Clinical Trials Logo

Airway Morbidity clinical trials

View clinical trials related to Airway Morbidity.

Filter by:

NCT ID: NCT02877940 Completed - Airway Morbidity Clinical Trials

Comparison of ProSeal Laryngeal Mask Airway, LTS-D and I-gel in Mechanically Ventilated Patients

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

The Aim of the study is to compare the clinical performance of p-LMA, i-gel and LTS-D in terms of the efficacy and safety in anaesthetized patient on Mechanical ventilation undergoing elective surgical procedure.

NCT ID: NCT02820792 Completed - Airway Morbidity Clinical Trials

Non-Crossover Study of the LMA Protector Versus Ambu AuraGain

Start date: September 2016
Phase: N/A
Study type: Interventional

The LMA ProtectorTM is a new extraglottic airway device which brings together features of both the LMA ProSealTM (high seal cuff, gastric access and bite block - to facilitate ventilation, airway protection and airway obstruction, respectively) and the LMA UniqueTM (single use - prevention of disease transmission). In the following randomized study the investigators test the hypothesis that ease of insertion, oropharyngeal leak pressure, fiberoptic position and ease of gastric tube placement differ between the LMA ProtectorTM and the Ambu AuraGainTM in paralyzed, anesthetized patients.

NCT ID: NCT02611986 Completed - Airway Morbidity Clinical Trials

Evaluation of Video Laryngoscopy (Video Macintosh-blade) and Direct Laryngoscopy (EMMA-Study)

EMMA
Start date: November 11, 2015
Phase: N/A
Study type: Interventional

A randomized controlled prospective study of laryngoscopy and intubation success comparing direct laryngoscopy and the McGrath® Mac videolaryngoscope.

NCT ID: NCT02572232 Completed - Emergencies Clinical Trials

Supraglottic Airway Devices in Pediatric Difficult Airway Situations

Start date: September 1, 2016
Phase: N/A
Study type: Interventional

The purpose of the study is to compare three supraglottic airway devices (Combitube, Easytube, laryngeal mask airway) to endotracheal intubation in a simulated difficult airway scenario in a pediatric manikin.

NCT ID: NCT02531256 Completed - Airway Morbidity Clinical Trials

An Investigation of a New Laryngeal Mask Airway LMA Protector

LMA
Start date: January 2014
Phase: N/A
Study type: Interventional

Evaluation of LMA Protector

NCT ID: NCT02359630 Completed - Airway Morbidity Clinical Trials

Multicenter Study of EasyTube® Compared to Endotracheal Tube in General Anesthesia

EasyTube
Start date: January 2005
Phase: Phase 3
Study type: Interventional

Evaluation of the EzT in comparison with the endotracheal tube (ETT) for its use during general anesthesia.

NCT ID: NCT02348736 Completed - Airway Morbidity Clinical Trials

Comparison of SensaScope Intuboscope and McGrath Series 5 for Endotracheal Intubation

SensaScope
Start date: January 2015
Phase: N/A
Study type: Interventional

A randomized controlled prospective study of laryngoscopy and intubation time comparing SensaScope and the McGrath® Series 5 video laryngoscope.

NCT ID: NCT02300337 Completed - Airway Morbidity Clinical Trials

Comparison of Reduced Cuff-pressure of the Laryngeal Tube Under General Anesthesia

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

Optimization the cuff pressure of the laryngeal tube (LT) in relation of the mechanical ventilation, and the reduction of potential leakage mucosal trauma. Comparison of the tightness of LT between the filling volume specified by the manufacturer (connectors are color coded syringe and blocker), 60cmH₂O, 50cmH₂O, 40cmH₂Ound 30cmH₂O. The measurement of the leakage occurs in ml / kg body weight.

NCT ID: NCT02048657 Completed - Airway Morbidity Clinical Trials

The Effectiveness of Foley Airway Stylet Tool on Proseal LMA Insertion

Start date: March 2008
Phase: N/A
Study type: Interventional

Due to its soft cuff easily folded to impede ProSeal LMA insertion, many tools are developed. The aim of the study is to investigate the efficiency of ProSeal LMA insertion guided by a soft, direct optical Foley airway stylet tool (FAST) and compared with the standard introducer-tool (I-Tool).

NCT ID: NCT02026882 Completed - Airway Morbidity Clinical Trials

Supreme LMA Use in Urgent Caesarean Section

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

The Supreme Laryngeal Mask Airway (SLMA) is a single use supraglottic device that provides a good seal for positive pressure ventilation and good first attempt insertion rate of 98% in low risk patients undergoing elective Caesarean section. It has a double aperture design that facilitates the introduction of an orogastric tube to aspirate gastric contents. The primary study hypothesis is the first attempt insertion success rate of SLMA use in urgent Caesarean section.