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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05347680
Other study ID # 0132-16
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 19, 2019
Est. completion date January 18, 2021

Study information

Verified date April 2022
Source Bnai Zion Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The intubating Laryngeal Tube Suction-Disposable is a new version of the Laryngeal Tube-Suction. It has a ventilator channel with a 13.5mm internal diameter, which enables the passage of an Endotracheal Tube with fiberoptic guidance. This study was designed to assess the Time fiberoptic endotracheal intubation using iLTS-D, in comparison with the and Ambu® AuraGain™ in adult patients.


Description:

The intubating Laryngeal Tube Suction-Disposable is a new version of the Laryngeal Tube-Suction. It has a ventilator channel with a 13.5mm internal diameter, which enables the passage of an Endotracheal Tube with fiberoptic guidance. This study was designed to assess the Time of fiberoptic endotracheal intubation using iLTS-D, in comparison with the and Ambu® AuraGain™ in adult patients. Detailed Description: The intubating Laryngeal Tube Suction-Disposable (iLTS-D) (VBM Medizintechnik GmbH, 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) with fiberoptic guidance. Similarly as in to the LTS-D, the iLTS-D also has a separate channel for the purpose of placement of gastric tubes placement up to a size of 18 Fr. The iLTS-D comes in one size. According to the depth of insertion, this device is equivalent to size 4 for patients height 175 to 190 cm tall, or size 5 for patients taller than 190 cm. The iLTS-D is provided by the manufacturer with a compatible 7.5 mm ETT and with a plastic stabilizer for removal of the device. The current randomized study was designed to assess the success rate fiberoptic endotracheal intubation using iLTS-D, in comparison with the and Ambu® AuraGain™ in adult patients under general anesthesia


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date January 18, 2021
Est. primary completion date January 15, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - American Society Anesthesiology I and II Exclusion Criteria: - Difficult intubation - Cervical pathology - pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Intubating Laryngeal Tube Suction
Intubating Laryngeal Tube Suction
Ambu AuraGain Laryngeal Mask
Ambu AuraGain Laryngeal Mask

Locations

Country Name City State
Israel Luis A Gaitini M.D. Haifa

Sponsors (1)

Lead Sponsor Collaborator
Bnai Zion Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time to perform fiberoptic intubation through supraglottic device in second Time to perform endotracheal fiberoptic intubation through supraglottic device in second 120 seconds
Secondary Success to obtain fiberoptic intubation through supraglottic device in second Success to obtain endotracheal fiberoptic intubation through supraglottic device in second 120 seconds
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