A study to compare dexmedetomidine with clonidine in decreasing agitation in children following palatoplasty.
Not Applicable
- Registration Number
- CTRI/2021/09/036261
- Lead Sponsor
- il
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All ASA 1 patients between the age of 6 months and 6 years coming for palatoplasty surgery whose parents are willing to give consent will be enrolled.
Exclusion Criteria
Parentâ??s refusal to consent, ASA 2 or above, upper respiratory tract infection, cardiac abnormality, major other systemic illness, coagulopathy, known allergy to alpha agonist agents will be excluded
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparing incidence of emergence agitation of dexmedetomidine with clonidineTimepoint: Emergence agitation will be assessed with FLACC score and Pediatric Anesthesia Emergence Delirium Scale every 5 min from the time of shifting to PACU until discharged
- Secondary Outcome Measures
Name Time Method Assessment of FLACC score, PAED scale, time to discharge in PACU, amount of rescue analgesics needed in PACUTimepoint: Emergence agitation will be assessed with FLACC score and Pediatric Anesthesia Emergence Delirium Scale every 5 min from the time of shifting to PACU until discharged