Trials / Unknown
UnknownNCT02884843
The New Intubating Laryngeal Tube Suction-Disposable
A Comparative Randomized Prospective Study Between the New Intubating Laryngeal Tube Suction-Disposable and the Ambu AuraGain in Blind and Fibreoptic-guided Intubation
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- Bnai Zion Medical Center · Other Government
- Sex
- All
- Age
- 18 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
The study compares the intubating Laryngeal Tube Suction (iLTS-D) with the Ambu®AuraGain™ in blind and fibreoptic endotracheal intubation. The current randomized study is designed to assess the success rate of blind and fibreoptic endotracheal intubation using i-LTS-D, in comparison with the Air-Q, i-gel® and Ambu®AuraGain™ in an airway simulator. The investigators hypothesize that the iLTS-D and the Supreme Laryngeal Mask Airway will similarly perform during spontaneous ventilation despite differences in their structural design.
Detailed description
The intubating Laryngeal Tube Suction-Disposable (iLTS-D) (VBM Medizintechnik, Sulz, Germany) is a new updated version of the Laryngeal Tube-Suction Disposable (LTS-D). It has a ventilator channel with a 13.5mm internal diameter, which enables the passage of an Endotracheal Tube (ETT) either blindly or with fibreoptic guidance. Similarly to the LTS-D, the iLTS-D also has a separate channel for gastric tubes placement up to a size of 18 Fr. The current randomized study was designed to assess the success rate of blind and fibreoptic endotracheal intubation using iLTS-D, in comparison with the Ambu® AuraGain™ in adult patients under general anesthesia.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Intubation laryngeal Tube Suction | Intubation laryngeal Tube Suction |
| DEVICE | AuraGain Laryngeal Mask | AuraGain Laryngeal Mask |
Timeline
- Start date
- 2016-08-01
- Primary completion
- 2016-08-01
- Completion
- 2017-07-01
- First posted
- 2016-08-31
- Last updated
- 2016-08-31
Source: ClinicalTrials.gov record NCT02884843. Inclusion in this directory is not an endorsement.