RecruitingPhase 1Phase 2NCT06545890
Ketofol Versus Dexmedetomidine for Prevention of Emergence Delirium in Pediatric Patients Undergoing Squint Surgeries
Ketofol Versus Dexmedetomidine for Prevention of Emergence Delirium in Pediatric Patients Undergoing Squint Surgeries: A Randomized Controlled Study.
Sponsor
Cairo University
Enrollment
46 participants
Start Date
Aug 10, 2024
Study Type
INTERVENTIONAL
Conditions
Summary
The aim of the study is to compare the effectiveness of ketofol for the prevention of emergence delirium in pediatric patients undergoing squint surgery, in comparison to dexmedetomidine.
Eligibility
Min Age: 2 YearsMax Age: 6 Years
Inclusion Criteria4
- All pediatric patients aged 2 to 6 years.
- Both sexes.
- ASA physical status I and II.
- Patients undergoing squint surgery.
Exclusion Criteria3
- Refusal of parents.
- Patient sensitivity to any of the study medications.
- Known neurological disease that can affect the assessment of ED postoperatively.
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Interventions
DRUGKetamine
continous infusion during surgery
DRUGDexmedetomidine
continous infusion during surgery
Locations(2)
View Full Details on ClinicalTrials.gov
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NCT06545890
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