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.
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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

Elif Şule Özdemir Sezgi

00905059209638

elifsule-91@hotmail.com

CONTACT

Aslı Dönmez

00905322256473

aslidonmez@hotmail.com

CONTACT