Use of Lidocaine in Rapid Sequence Induction
Information source: University of Athens
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Hemodynamic Response
Intervention: Lidocaine (Drug); Placebo (Drug)
Phase: N/A
Status: Completed
Sponsored by: University of Athens
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.
Clinical Details
Official title: Impact of Lidocaine on Anesthetic Depth During Rapid Sequence Induction
Study design: Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor)
Primary outcome: BIS changes after lidocaine administration in rapid sequence induction
Secondary outcome: change in blood pressurechange in Heart rate
Eligibility
Minimum age: 20 Years.
Maximum age: 70 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- reason for rapid sequence induction (emergency, reflux),
- ASA I-II,
- no antihypertensive drugs,
- no antiarrhythmic drugs
Exclusion Criteria :
Locations and Contacts
Aretaieio Hospital, University of Athens, Athens, Attiki 11528, Greece
Additional Information
Starting date: October 2008
Last updated: August 23, 2011
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