Premedication in Children: a Clinical Trial Comparing Oral Ketamine and Oral Clonidine With Respect to Sedation Level and Opioid Consumption in Pediatrics Undergoing Elective Lower Abdominal Day-case Surgery.
Recruiting
N/A
Interventional Study
Pediatric Sedation
Clonidine Sedation
Ketamine Sedation
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 3 – 12
- Sex
- Any
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 84 (estimated)
- Sponsor
- Cairo University · Other
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About This Trial
Aim of the work Is to compare between oral ketamine and oral clonidine regarding the level of sedation pre and postoperatively in addition the need of opioids administration intraoperative in children undergoing elective lower abdominal day-case surgery.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Children aged between 3 to 12 years old of both sexes undergoing elective lower abdominal day-case surgery such as: oblique inguinal herniorrhaphy, hypospadias correction and circumcision.
* ASA I and II
Exclusion Criteria:
* Parents refusal.
* ASA risk score \>II
* Heart, l…
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