Comparing inhaled Dexmedetomidine against inhaled Midazolam to suppress anxiety in children.
Phase 1
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/08/056083
- Lead Sponsor
- Daryl Phils Joe
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA GRADE 1 AND 2
Elective surgeries under general anaesthesia.
Exclusion Criteria
Emergency surgeries.
Known allergies to dexmedetomidine and/or midazolam.
Significant organ dysfunction.
Cardiac dysrhythmias, Congenital heart disease.
Mentally challenged.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Compare parent separation anxiety in paediatric population receiving nebulised dexmedetomidine or nebulised midazolam preoperatively.Timepoint: 30 minutes prior to surgery
- Secondary Outcome Measures
Name Time Method To compare emergence reaction in paediatric population receiving nebulised dexmedetomidine or nebulised midazolam preoperatively.Timepoint: immediately after surgery to 30 minutes after surgery;To compare mask acceptance in paediatric population receiving nebulised dexmedetomidine or nebulized midazolam preoperativelyTimepoint: On start of anaesthetic procedures.