Comparision of oral and intranasal routes for midazolam premedication in paediatric patients
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/08/055961
- Lead Sponsor
- Shaji P John
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Paediatric patients aged between 1-10 years scheduled for elective surgeries.
American Society of Anaesthesiologist (ASA) grade 1 and 2.
Exclusion Criteria
Children with central nervous system disorder, epilepsy, developmental delay, mental
retardation.
Known hypersensitivity and contraindication to drugs used.
History of significant cardiac, respiratory, renal, hepatic disease.
Patients having nasal infection, nasal pathology and taking any other sedative drugs.
Parental refusal.
Anticipated difficult airway.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To find out the level of sedation (sedation score) & acceptance of the route of administration of <br/ ><br>the drug between the two groups. <br/ ><br>To find out the ease of parental separation (separation score) between the two groups.Timepoint: Grades of sedation at - <br/ ><br>0 mins <br/ ><br>5 mins <br/ ><br>15 mins <br/ ><br>20 mins
- Secondary Outcome Measures
Name Time Method To assess hemodynamic stability, recovery characteristics (recovery score) & time taken to <br/ ><br>achieve satisfactory sedation between the two groups.Timepoint: Present or not present