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Your journey
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More info
You can access this
clinical trial
if you have
Adverse Anesthesia Outcome
and you are
between 18 and 90
years old
The phase for this study is not defined.
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The purpose

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.

Provided treatments

  • Device: Intubation laryngeal Tube Suction
  • Device: AuraGain Laryngeal Mask

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT02884843. The sponsor of the trial is Bnai Zion Medical Center and it is looking for 60 volunteers for the current phase.
Official trial title:
A Comparative Randomized Prospective Study Between the New Intubating Laryngeal Tube Suction-Disposable and the Ambu AuraGain in Blind and Fibreoptic-guided Intubation