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Clinical Trial Summary

Introduction: Although inflating tracheal cuff using lidocaine is effective for cough suppression, it may pressure tracheal cuff too much. Intravenous continuous infusion of lidocaine has emerged recently for most general anesthesia in the context of opioid-sparing anesthesia for cancer, but the 95% effective dose (ED95) for cough suppression during anesthesia emergence is not determined yet. Objective: the objectives of this study are to determine the ED95 of continuous infusion lidocaine for suppressing cough reflex during extubation by sex and age group.


Clinical Trial Description

Ideal patient weight in kg will be considered.

Initial dose will be 0.5mg/kg.h and dose-change steps of 0.5mg/kg.h will occur depending on the incidence of emergence cough in the previous patient of the same group:

- It will increase if coughed in a probability of 95%

- It will decrease if not coughed in a probability of 5%.

- It will remain the same otherwise. Maximum dose will be 3mg/kg.h. All patients will receive remifentanil 0.025mcg/kg.min continuous infusion until extubation.

Patients groups will be determined by sex and age group (18-60 or >60 years old), therefore, four independent groups will be studied:

- Female 18 to 60 years old

- Male 18 to 60 years old

- Female > 60 years old

- Male > 60 years old ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03805282
Study type Interventional
Source Brasilia University Hospital
Contact Gabriel MN Guimaraes, MSc
Phone +55 61 996455997
Email gabrielmng@gmail.com
Status Recruiting
Phase Phase 3
Start date March 1, 2018
Completion date December 31, 2019

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