The effect of Lidocaine on control of emergence agitation due to Sevoflurane
Phase 3
- Conditions
- Agitation.Restlessness and agitation
- Registration Number
- IRCT2013072914199N1
- Lead Sponsor
- Research Council of Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Parent willingness to participate in the study and informed consent, Age group: 12 to 36 months, Retinoblastoma eyes Exclusion criteria: A history of seizures, Liver disease, Kidney disease, Heart disease, Having a cold during the current week, Sensitivity to Lidocaine, Intense crying
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Agitation. Timepoint: The scores were recorded every 10 minutes (In the first 30 minutes after entering into recovery), since the children transferred to recovery. Method of measurement: Anesthesiologist divided children into 5 levels based on agitation: 1. Asleep; 2. Awake and calm; 3. Irritable or consolable crying; 4. Inconsolable crying; and 5. Severe restlessness.
- Secondary Outcome Measures
Name Time Method ausea and vomiting. Timepoint: The symptoms were recorded every 10 minutes (In the first 30 minutes after entering into recovery), since the children transferred to recovery. Method of measurement: Observation.