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Use of Lidocaine in Rapid Sequence Induction

N

National and Kapodistrian University of Athens

Status

Completed

Conditions

Hemodynamic Response

Treatments

Drug: Placebo
Drug: Lidocaine

Study type

Interventional

Funder types

Other

Identifiers

NCT01238718
lidocaine3

Details and patient eligibility

About

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.

Enrollment

76 estimated patients

Sex

All

Ages

20 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

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

Exclusion Criteria :

Trial design

76 participants in 2 patient groups, including a placebo group

lidocaine
Active Comparator group
Treatment:
Drug: Lidocaine
normal saline
Placebo Comparator group
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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