Comparison of the efficacy of oral and intranasal midazolam premedication on sedation before undergoing MRI in childre
Phase 3
Recruiting
- Conditions
- Preanesthetic sedation.Sedative, hypnotic, or anxiolytic related disorders
- Registration Number
- IRCT20151221025641N8
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
The patient is classified as ASA class 1 to 2 according to the American Society of Anesthesiologists;
The patient's age is between 6 months to 6 years;
The patient is a candidate for MRI under anesthesia;
Exclusion Criteria
The patient has upper gastrointestinal tract problems;
The patient has an active infection;
The patient has structural disorders of the upper respiratory system;
The patient is cyanotic;
Having a history of drug allergy to benzodiazepines;
Severe crying and restlessness of the child immediately before administering the medicine;
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sedation scale. Timepoint: 0, 5, 10, 15 and 20 minutes after receiving the intervention. Method of measurement: Scoring system and clinical assessment.
- Secondary Outcome Measures
Name Time Method Parental separation anxiety scale. Timepoint: 20 minutes after receiving the intervention. Method of measurement: Scoring system and clinical assessment.;Mask acceptance score. Timepoint: 20 minutes after receiving the intervention. Method of measurement: Scoring system and clinical assessment.;Recovery score. Timepoint: Recovery time. Method of measurement: Scoring system and clinical assessment.;Agitation score. Timepoint: At discharge. Method of measurement: Scoring system and clinical assessment.