Sedative effect of ketamine, midazolam and oral chloral hydrate in childre
Not Applicable
- Conditions
- Oral sedation in children.Dissociative anaesthesia and sensory loss
- Registration Number
- IRCT2015010612642N9
- Lead Sponsor
- Vice Chancellor for Research and Technology Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
inclusion criteria: Candidate for CT scan; candidate for audiometry; age between 2 to 10 years old; ASA I,II
exclusion criteria: History of taking sedative drugs, history of drug abuse, history of taking anticonvulsants, history of allergy
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time of separating from parents. Timepoint: Every 5 min after administration. Method of measurement: Based on the examination by the research team.;Sedation. Timepoint: Every 5 min after administration. Method of measurement: Based on the examination by the research team based on sedatin score.;Anxiety. Timepoint: Every 5 min after administration. Method of measurement: Based on the examination by the team on the anxiety sedation table.;The children move during the procedure. Timepoint: 0,15 and 30 minute after drug administration. Method of measurement: Based on the examination by the team on the anxiety sedation table.
- Secondary Outcome Measures
Name Time Method Children waking time. Timepoint: Since taking oral medication. Method of measurement: Based on the examination by the team in minutes.;Nausea. Timepoint: After taking oral medication. Method of measurement: Questions from Parents.