Comparative Assessment of Oral Premedication Regimens in Pediatric Ambulatory Surgery
Recruiting
N/A
Interventional Study
Pediatric Anesthesia
Premedication
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 4 – 12
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 135 (estimated)
- Sponsor
- Diskapi Yildirim Beyazit Education and Research Hospital · Government
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About This Trial
This prospective, three-arm study aims to evaluate the effects of different oral premedication regimens on venipuncture tolerance in pediatric patients undergoing ambulatory surgery. Children aged 4-12 years scheduled for elective day-case procedures will receive oral midazolam alone, midazolam combined with ibuprofen, or midazolam combined with ketamine prior to anesthesia induction. The primary …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Pediatric patients aged 4-12 years
* American Society of Anesthesiologists (ASA) physical status I-II
* Scheduled for elective ambulatory (day-case) surgery
* Eligible to receive oral premedication
* Cognitive ability sufficient to complete behavioral and pain scale assessment…
Contacts