CTRI/2022/09/045492
Not yet recruiting
Phase 3
A comparative study to evaluate the analgesic efficacy and safety of caudal versus intranasal dexmedetomidine as an adjuvant to caudal ropivacaine in paediatric patients undergoing infraumbilical surgeries : A Double blind randomised controlled study
All India Institute of Medical Sciences New Delhi0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- All India Institute of Medical Sciences New Delhi
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •patient Aged 1\-8 years,ASA physical status I/II, undergoing infraumbilical surgeries under general anaesthesia
Exclusion Criteria
- •1\.Parental /guardian refusal for inclusion in the study
- •2\.Known allergy to amide local anaesthetics or dexmedetomidine.
- •3\.Pre\-existing cardiovascular, respiratory or neurological disease
- •4\.History of developmental delay or mental retardation which could make observational pain intensity assessment difficult
- •5\.Children with conduction blocks
- •6\.Known or suspected coagulopathy
- •7\.Anatomical abnormalities of spine and sacrum.
- •8\.Local infection at caudal puncture site
- •9\.Rhinitis and nasal polyp
- •10\.Patients with age \< 1 years and \>7 years
Outcomes
Primary Outcomes
Not specified
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