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Clinical Trials/NCT01238718
NCT01238718CompletedNot Applicable

Impact of Lidocaine on Anesthetic Depth During Rapid Sequence Induction

University of Athens1 site in 1 country76 target enrollmentStarted: October 2008Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
76
Locations
1
Primary Endpoint
BIS changes after lidocaine administration in rapid sequence induction

Study Overview

Brief 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
20 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • reason for rapid sequence induction (emergency, reflux),
  • ASA I-II,
  • no antihypertensive drugs,
  • no antiarrhythmic drugs
  • Exclusion Criteria :

Exclusion Criteria

  • Not provided

Arms & Interventions

lidocaine

Active Comparator

Intervention: Lidocaine (Drug)

normal saline

Placebo Comparator

Intervention: Placebo (Drug)

Outcomes

Primary Outcomes

BIS changes after lidocaine administration in rapid sequence induction

Time Frame: change from baseline in BIS values during 10 minutes

Secondary Outcomes

  • change in blood pressure(change from baseline in blood pressure during 10 minutes)
  • change in Heart rate(change from baseline in heart rate durng 10 minutes)

Investigators

Sponsor
University of Athens
Sponsor Class
Other

Study Sites (1)

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