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RecruitingNCT07323485

Inflammatory Biomarkers and Postoperative Delirium in Pediatric Circumcision

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Trial Parameters

ConditionPostoperative Delirium
SponsorAnkara Etlik City Hospital
Study TypeOBSERVATIONAL
PhaseN/A
Enrollment140
SexMALE
Min Age2 Years
Max Age12 Years
Start Date2026-01-18
Completion2026-06-10
Interventions
Measurement of Preoperative Inflammatory Biomarkers

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Brief Summary

Postoperative delirium may occur in children after general anesthesia, even following short procedures such as circumcision. Preoperative systemic inflammation has been associated with postoperative delirium in adults, but data in pediatric patients are limited. This prospective observational study aims to evaluate the association between preoperative inflammatory biomarkers and postoperative delirium in children aged 2-12 years undergoing elective circumcision under general anesthesia. Inflammatory biomarkers derived from routine complete blood count parameters, including NLR, PLR, MLR, SII, and SIRI, will be analyzed. Postoperative delirium will be assessed using the Pediatric Anesthesia Emergence Delirium (PAED) scale in the post-anesthesia care unit. The relationship between inflammatory biomarkers and delirium development and severity will be evaluated. This study seeks to identify simple preoperative markers that may help predict postoperative delirium risk in pediatric patients.

Eligibility Criteria

Inclusion Criteria: * Children aged 2-12 years. * Patients scheduled to undergo elective circumcision under general anesthesia. * Patients classified as ASA physical status I-II. * Patients whose parents or legal guardians provide written informed consent, and whose age-appropriate verbal assent is obtained from the child. * Patients in whom anesthesia and surgical procedures are performed according to standard institutional protocols throughout the study period. Exclusion Criteria: * Children with a history of neurological or psychiatric disorders (e.g., epilepsy, developmental delay, autism spectrum disorder, anxiety disorders). * Patients classified as ASA physical status III-IV. * Patients with incomplete preoperative laboratory data or with hematological or hormonal disorders that may affect inflammatory parameters. * Patients who develop excessive sedation after premedication or whose preoperative assessment cannot be completed. * Patients with protocol deviations during surgery

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