Effect of Preoperative Fasting Duration on Postoperative Pain and Emergence Agitation in Pediatric Patients Undergoing Urogenital Surgery

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age2-8
SponsorTC Erciyes University

About this trial

This study aims to evaluate the effect of preoperative fasting duration on postoperative pain and emergence agitation in pediatric patients undergoing urogenital surgery.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age between 2 and 8 years

ASA physical status I-II

Scheduled for elective urogenital surgery

Disqualifiers

ASA physical status ≥ III

Malnutrition

Neuropsychiatric disorders

Respiratory tract infection

Trial population

The study population consists of pediatric patients aged 2-8 years with ASA physical status I-II undergoing elective urogenital surgery at a single tertiary care university hospital. Eligible participants will be consecutively recruited and assessed preoperatively together with their parents or legal guardians.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

250 Participants
are grouped into 1 trial group
Group A: İn Children Aged 2-8 Years Undergoing Elective Urogenital Surgery:

Trial outcomes

Primary outcomes

1

Postoperative agitation assessed using the Pediatric Anesthesia Emergence Delirium (PAED) scale in the post-anesthesia care unit

Each item is scored from 0 to 4. Items 1-3 (Positive behaviors - reverse scored): The child makes eye contact with the caregiver The child's actions are purposeful The child is aware of his/her surroundings 4 = Not at all 3 = Just a little 2 = Quite a bit 1 = Very much 0 = Extremely Items 4-5 (Negative behaviors): The child is restless The child is inconsolable 0 = Not at all 1. = Just a little 2. = Quite a bit 3. = Very much 4. = Extremely Total Score Range: 0-20 Interpretation * 10 → Suggestive of emergence delirium * 12 → Strongly indicative / more severe delirium

Time frame
One day

Secondary outcomes

Other outcomes

Sponsors and contacts

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