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Comparison of Direct Laryngoscopy With Blind Intubation Via Intubating Laryngeal Mask Airway

B

Bnai Zion Medical Center

Status

Unknown

Conditions

Adverse Anesthesia Outcome

Treatments

Device: Intubating Laryngeal Mask

Study type

Interventional

Funder types

Other

Identifiers

NCT02884869
BnaiZionMC-16-LG-006

Details and patient eligibility

About

Control the airways by endotracheal intubation is an important part of treatment for a trauma casualty. The use of the Laryngeal Mask Airway for fast control of the airway is known for many years. The aim of this study is to examine the effectiveness of the Intubating Laryngeal Mask Airway to achieve a definitive airway by unskilled practitioners.

The hypothesis is that definitive airway obtaining with Intubating Laryngeal Mask Airway will be more success and faster compared to the standard way of direct laryngoscope.

Full description

Control the airways and respiration are an important part of treatment for a trauma casualty. Tracheal intubation an action that allows the insertion of a tube through the vocal cords and fixation by the balloon inflation is a definitive airway. The use of the Laryngeal Mask Airway for fast control of the airway is known for many years. The Laryngeal Mask Airway and others similar devices are known as Supraglottic Airway Devices and are inserted blind in the oropharynx and allow a fast oxygenation and ventilation of the patients.The aim of this study is to examine the effectiveness of the Laryngeal Mask Airway to achieve a definitive airway by unskilled practitioners in anesthetized patients with the head in neutral position (trauma model)

The hypothesis is that definitive airway obtaining with Intubating Laryngeal Mask Airway will be more success and faster compared to the standard way of direct laryngoscope. If the hypothesis is proven, this research will be very important implications for the management of the airway describing pre-hospital and in particular military scenarios.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • American Society Anesthesiology class I and II

Exclusion criteria

  • Difficult airway
  • Cervical pathology
  • Full stomach

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

60 participants in 2 patient groups

Intubating laryngeal Mask
Experimental group
Description:
Intubating laryngeal Mask
Treatment:
Device: Intubating Laryngeal Mask
Direct laryngoscopy
Active Comparator group
Description:
Intubating laryngeal Mask
Treatment:
Device: Intubating Laryngeal Mask

Trial contacts and locations

0

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Central trial contact

Luis A Gaitini, M.D.; Mostafa Somri, M.D.

Data sourced from clinicaltrials.gov

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