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Effect of intravenous lidocaine on propofol narcosis

Conditions
the effects of intravenous application of lidocaine on the Cp50 during propofol narcosis should be investigated
Therapeutic area: Body processes [G] - Chemical Phenomena [G02]
Registration Number
EUCTR2011-000022-29-AT
Lead Sponsor
Medizinische Universität Wien
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
36
Inclusion Criteria

operation under general anaesthesia
insertion of LMA possible
age 20-60 years
ASA 1-2
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 36
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

premedication
tracheal intubation
allergy to lidocaine
body mass index > 30
history of esophageal reflux, hiatal hernia, peptic ulcer disease
significant cardiovascular, respiratory, renal or hepatic disease
history of alcohol or drug abuse
pregnancy
arrhythmias
epilepsy

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: to evaluate the effect of intravenous lidocaine on the Cp50 of propofol;Secondary Objective: to evaluate the effect of intravenous lidocaine on BIS and hemodynamics;Primary end point(s): movement or no movement at skin incision;Timepoint(s) of evaluation of this end point: skin incision
Secondary Outcome Measures
NameTimeMethod
Secondary end point(s): BIS and hemodynamic changes at skin incision;Timepoint(s) of evaluation of this end point: skin incision
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