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Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness of nebulized lidocaine before Endotracheal suctioning (ETS) compared to instilled lidocaine and the effectiveness of aerosolized lidocaine versus instilled normal saline before ETS in attenuating the increase of intracranial pressure (ICP) in severe head injured children and to evaluate the feasibility of a trial involving instilled lidocaine and aerosolized lidocaine for the management of ETS and to evaluate the safety of nebulized lidocaine in traumatic brain injury (TBI) compared to instilled lidocaine and instilled sodium chloride (NS).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05058677
Study type Interventional
Source The University of Texas Health Science Center, Houston
Contact Sheikh S Ahmed, MD
Phone (713) 500-5553
Email [email protected]
Status Not yet recruiting
Phase Phase 4
Start date October 1, 2021
Completion date June 30, 2022

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