Actively Recruiting
Effect of Preoperative Inflammatory Biomarkers on Postoperative Delirium in Children Undergoing Circumcision
Led by Ankara Etlik City Hospital · Updated on 2026-02-20
140
Participants Needed
1
Research Sites
6 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Postoperative delirium can occur in children after general anesthesia, even following short procedures like circumcision. This observational study evaluates the link between preoperative inflammatory markers and postoperative delirium in children aged 2 to 12 years undergoing elective circumcision under general anesthesia. The study aims to find simple blood-based markers that might help predict the risk of delirium after surgery in pediatric patients. Blood samples will be taken before surgery to measure inflammatory biomarkers such as neutrophil-to-lymphocyte ratio, platelet-to-lymphocyte ratio, systemic immune-inflammation index, monocyte-to-lymphocyte ratio, and systemic inflammation response index. These markers will be analyzed in relation to the development and severity of delirium assessed within 2 hours after surgery using the Pediatric Anesthesia Emergence Delirium (PAED) scale. No experimental drugs or devices will be used; all procedures follow standard care protocols. Participants will be monitored in the post-anesthesia care unit, where delirium will be assessed shortly after surgery. Researchers will review blood test results and delirium scores to understand the relationship between inflammation and delirium severity. The main outcome measured is the incidence of delirium within 2 hours after surgery, with secondary outcomes focusing on the correlation between biomarker levels and delirium severity. The study is expected to finish by July 2026.
CONDITIONS
Brief Title
Inflammatory Biomarkers and Postoperative Delirium in Pediatric Circumcision
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children aged 2-12 years
- Scheduled for elective circumcision under general anesthesia
- Classified as ASA physical status I or II
- Parents or legal guardians provide written informed consent
- Age-appropriate verbal assent obtained from the child
- Anesthesia and surgery performed according to standard institutional protocols
You will not qualify if you...
- History of neurological or psychiatric disorders such as epilepsy, developmental delay, autism spectrum disorder, or anxiety disorders
- Classified as ASA physical status III or IV
- Incomplete preoperative laboratory data or hematological or hormonal disorders affecting inflammatory markers
- Excessive sedation after premedication or incomplete preoperative assessment
- Protocol deviations during surgery or anesthesia, including additional medications, prolonged surgery, or procedural changes due to complications
- Parents or legal guardians do not consent or decline participation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants have blood samples collected preoperatively to assess inflammatory biomarkers related to postoperative delirium.
1 visit (in-person)
Duration - Within 2 hours postoperatively
Participants are observed for emergence delirium and its severity within the first 2 hours after circumcision.
Continuous observation during recovery
Trial Site Locations
Total: 1 location
1
Ankara Etlik City Hospital
Altındağ, Ankara, Turkey (Türkiye)
Actively Recruiting
Research Team
A
Ahmet Murat Gül
A
Aslı Dönmez
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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