Efficacy of intravenous lidocaine 2% and propofol in preventing laryngospasm

Phase 2

Recruiting

• Conditions: laryngospasm and complications after tonsilectomy.; Laryngeal spasm; J38.5

• Registration Number: IRCT20120915010841N16
• Lead Sponsor: Hamedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 May 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 102

Inclusion Criteria

Aged 3-14 years old
Candidate for elective adenotonsilectomy
Parental Satisfaction

Exclusion Criteria

Those who are reluctant to continue to participate in the study
History of Cardio-pulmonary disease
Recent infection of the upper respiratory tract and febrile illnesses
History of allergy to eggs, soy, lidocaine and propofol
difficult intubation
Corticosteroid use

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
aryngospasm. Timepoint: 1, 3, 5, 10 and 15 minutes after extubation. Method of measurement: Observation.

Secondary Outcome Measures

Name	Time	Method
ausea & vomiting. Timepoint: After surgery. Method of measurement: Observation.;Systolic and Diastolic Blood Pressure. Timepoint: Every two minutes for 10 minutes and then every 10 minutes to 60 minute. Method of measurement: Non-invasive automatic barometric device.;Heart Rate. Timepoint: Every two minutes for 10 minutes and then every 10 minutes to 60 minute. Method of measurement: Non-invasive automatic barometric device.