Comparing one drug used to sedate and decrease anxiety in children using two different routes posted for surgery under general anaesthesia
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/12/038369
- Lead Sponsor
- ONE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
pediatric age group 1 -5 years
ASA grade 1 and 2
patients undergoing elective surgeries under general anaesthesia
Exclusion Criteria
refusal of informed consent
haemodynamic instability
emergency surgeries
fever or infection
patient with recent history and active nasal bleeding
patient with nasal mass
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method to compare the sedation achieved at 30 minutes after administration of midazolam either through oral route or intranasal routeTimepoint: BASELINE TO 30 MINUTES AFTER INTRODUCTION OF DRUG
- Secondary Outcome Measures
Name Time Method to evaluate quality of parental separation <br/ ><br>to evaluate acceptance of drug through oral or nasal route <br/ ><br>to evaluate ease of mask acceptance during preoxygenationTimepoint: baseline <br/ ><br>TILLN 20 MINUTES AFTER INTRODUCTION OF THE DRUG