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NCT04238351 Clinical Trial

Transnasal Humidified Rapid Insufflation System for Intubation

Hypoxemia Clinical Trial

Official title:
Effect of Transnasal Humidified Rapid Insufflation Ventilator Exchange During Anesthesia Induction With Double Lumen Endotracheal Tube

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04238351
Other study ID # Gil2019-2
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date February 25, 2020
Est. completion date December 31, 2020

Study information
Verified date February 2020
Source Gachon University Gil Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Transnasal humidified rapid insufflation ventilator exchange (THRIVE) or not during the anesthesia induction

Description:

Control group-usual mask ventilation during apnea for anesthetic intubation and check tube positioning THRIVE group-applying THRIVE during apnea for anesthetic intubation and check tube positioning

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 80
Est. completion date December 31, 2020
Est. primary completion date November 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients who scheduled for elective lung surery with one lung ventilation

Exclusion Criteria:

- suspicious difficult intubation (BMI >35kg/m2, mouth opening < 3 finger, Mallampati G >3), Room air SpO2 < 90%, active pulmonary infection, emergency operation, pregnancy

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Transnasal humidified rapid insufflation ventilator exchange
applying 40L of oxygen for 1min and afte that increase oxygen flow up to 70L for 1 min.
• Conventional face mask
applying oxygen using usual face mask

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Gachon University Gil Medical Center

Outcome
Type Measure Description Time frame Safety issue
Primary Desaturation number of patients who experienced SpO2 under 93% during the anesthesia induciton
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