Actively Recruiting

Age: 2Years - 12Years
MALE
Healthy Volunteers
NCT07323485

Inflammatory Biomarkers and Postoperative Delirium in Pediatric Circumcision

Led by Ankara Etlik City Hospital · Updated on 2026-02-20

140

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Inflammatory Biomarkers and Postoperative Delirium in Pediatric Circumcision

Who Can Participate

Age: 2Years - 12Years
MALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Children aged 2-12 years
  • Scheduled for elective circumcision under general anesthesia
  • Classified as ASA physical status I-II
  • Written informed consent from parents or legal guardians
  • Age-appropriate verbal assent obtained from the child
  • Anesthesia and surgery performed according to standard institutional protocols
Not Eligible

You will not qualify if you...

  • History of neurological or psychiatric disorders (e.g., epilepsy, developmental delay, autism spectrum disorder, anxiety disorders)
  • Classified as ASA physical status III-IV
  • Incomplete preoperative laboratory data or hematological/hormonal disorders affecting inflammatory parameters
  • Excessive sedation after premedication or incomplete preoperative assessment
  • Protocol deviations during surgery or anesthesia (e.g., additional medications, prolonged surgery, procedural changes due to complications)
  • Parents or legal guardians do not provide consent or decline participation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ankara Etlik City Hospital

Altındağ, Ankara, Turkey (Türkiye)

Actively Recruiting

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Research Team

A

Ahmet Murat Gül

CONTACT

A

Aslı Dönmez

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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