arynxmaske bei Kindern nach Atemwegsinfekt: Der Effekt topischer Anästhesie mit LidocainEffect of Lidocain-gel for laryngeal mask lubrification in pediatric patients after acute respiratory disease -

• Conditions: Acute respiratory diseases are common in pediatric patients scheduled for general anesthesia, and can cause perioperative problems up to 6 weeks after the acute respiratory infection. In the present double-blind, randomized study the effect of lidocain gel for laryngeal mask lubrification on the rate of perioperative respiratory adverse events is studied in pediatric patients with a recent history of respiratory infection and in patients without a history of respiratory infection.; MedDRA version: 9.1Level: LLTClassification code 10038700Term: Respiratory infection

• Registration Number: EUCTR2007-002314-19-AT
• Lead Sponsor: Medical University of Vienna, Department of Anesthesiology

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2007-09-13
• Last Update Posted: 19 March 2012

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: Male
• Target Recruitment: Not specified

Inclusion Criteria

patients: male, age 1 - 6, scheduled for circumcision, otherwise healthy
Are the trial subjects under 18? yes
Number of subjects for this age range:
F.1.2 Adults (18-64 years) no
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

all patients with indications for endotracheal intubation, patients with a history of allergies against local anesthetics

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Main Objective: Study the effect of topical anesthesia with lidocain gel for laryngeal mask lubrification on perioperative respiratory adverse events in pediatric patients undergoing general anesthesia with or without a recent history of acutes respiratory disease ;Secondary Objective: none;Primary end point(s): Sum of perioperative adverse respiratory events (Tait et al., Anesthesiology 2001)