CTRI/2022/04/042249
Completed
未知
Comparison of the efficacy of Intranasal Atomised Dexmedetomidine versus Intranasal Atomised ketamine as a premedicant for anxiolysis and sedation in paediatric population aged 1-10 years undergoing spinal dysraphism surgery - a randomised double blinded controlled trial.
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Ankur Luthra
- Enrollment
- 64
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •64 ASA I and II children aged between 1\-10years scheduled for spinal dysraphism surgery will be enrolled in this study.
Exclusion Criteria
- •Refusal of consent
- •Known allergy to dexmedetomidine or ketamine
- •ASA III or IV
- •Children with cardiac anomalies
- •Children with seizures
- •Children with upper respiratory tract infection
- •Children with liver disease
- •Children with mental retardation
- •Difficult cannulation (three or more attempts)
Outcomes
Primary Outcomes
Not specified
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