Clinical Trials Directory

Trials / Unknown

UnknownNCT02977559

A Study Between the Laryngeal Tube Suction-Disposable and the Ambu AuraGain in Pediatric Patients

A Comparative Randomized Prospective Study Between the New Laryngeal Tube Suction-Disposable and the Ambu AuraGain in Pediatric Patients

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Bnai Zion Medical Center · Other Government
Sex
All
Age
1 Year – 10 Years
Healthy volunteers
Not accepted

Summary

The study compared the Laryngeal Tube Suction Disposable (LTS-D) with the Disposable Laryngeal Mask Ambu® AuraGain™ (DLMA AG) during general anesthesia in pediatric patients. The investigators hypothesized that the LTS-D and the DLMA AG performed similarly during mechanical ventilation despite differences in their structural design.

Detailed description

The Laryngeal Tube Suction-Disposable (LTS-D, (VBM Medizintechnik GmbH, Sulz, Germany), is a second generation single-use supraglottic airway devices (SADs) with gastric access, for airway management in spontaneously and mechanically ventilated patients undergoing general anesthesia. The AuraGain is a second generation laryngeal mask, satisfying airway management needs by integrating gastric access and ventilation capability in an anatomically curved single-use device that facilitates rapid establishment of a safe airway. The two devices have now pediatric sizes. To date, there is no published data comparing the LTS-D and the DLMA AG during mechanical ventilation in pediatric patients. The investigators hypothesized that the LTS-D and the DLMA AG perform similarly during mechanical ventilation despite differences in their structural design. The chief aim of this prospective randomized study was to compare the LTS-D and the DLMA AG with respect to: 1. time to achieve an effective airway, 2. ease of insertion, 3. need for interventions to achieve an effective airway, 4. cuff seal (leak) pressure at an intracuff pressure of 60 cm H2O, 5. ventilatory variables during mechanical ventilation, 6. fiberoptic score, 7. gastric tube insertion and 8. adverse perioperative events.

Conditions

Interventions

TypeNameDescription
DEVICELaryngeal Tube Suction DisposableDevice for ventilation
DEVICELaryngeal Mask Airway AuraGainVentilation device

Timeline

Start date
2017-03-01
Primary completion
2017-04-01
Completion
2017-09-01
First posted
2016-11-30
Last updated
2016-12-01

Source: ClinicalTrials.gov record NCT02977559. Inclusion in this directory is not an endorsement.