Comparison of the effect of midazolam in oral and nebulized form
Phase 2
Recruiting
- Conditions
- This study is conducted for sedation in children undergoing eye surgeries. The entry criteria of our children should not have any underlying disease and be between 3 and 7 years old..
- Registration Number
- IRCT20230117057153N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
ASA I and II
Children aged 3 to 7 years
Eye surgery under general anesthesia
Exclusion Criteria
Patients with renal or hepatic dysfunction
History of midazolam allergy
History of asthma
Pre-existing neurologic disease
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Determining sedation level using RAMSAY score within 30 minutes after administration of nebulized vs oral midazolam in pediatric eye surgery patients. Timepoint: 30 minutes after drug administration. Method of measurement: RAMSAY sedation score (0-6).
- Secondary Outcome Measures
Name Time Method