Clinical Trials Directory

Trials / Completed

CompletedNCT01238718

Use of Lidocaine in Rapid Sequence Induction

Impact of Lidocaine on Anesthetic Depth During Rapid Sequence Induction

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
76 (estimated)
Sponsor
University of Athens · Academic / Other
Sex
All
Age
20 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Lidocaine has been shown to blunt the cardiovascular response to endotracheal intubation. The incidence of hypertension, tachycardia and dysrhythmias due to laryngoscopy may be increased in patients that receive rapid sequence induction and intubation, where opioids are spared and intravenous anesthetic agents are not titrated step by step. Our hypothesis was that lidocaine when administered intravenously in patients who undergo rapid sequence induction may not only blunt the hemodynamic response to intubation, but may also increase the anesthetic depth (as assessed by BIS), thus further reducing the possibility of hypertension, arrhythmias and also awareness.

Conditions

Interventions

TypeNameDescription
DRUGLidocainelidocaine 1.5 mg/kg intravenously
DRUGPlacebonormal saline

Timeline

Start date
2008-10-01
Primary completion
2011-07-01
Completion
2011-07-01
First posted
2010-11-11
Last updated
2011-08-24

Locations

1 site across 1 country: Greece

Source: ClinicalTrials.gov record NCT01238718. Inclusion in this directory is not an endorsement.