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Clinical Trials in Turkey / NCT07148063
Recruiting Observational

Inflammatory Biomarkers as Predictors of PONV Following Pediatric Orchiopexy

NCT07148063 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2025-09-08
Last updated
2025-09-09

Condition(s) studied

Pediatric AnesthesiaPostoperative Nausea and Vomiting (PONV)Inflammatory Biomarkers

Investigational drug(s) / intervention(s)

Measurement of Preoperative Inflammatory Biomarkers

Measurement of Preoperative Inflammatory Biomarkers: Blood samples will be collected preoperatively to measure inflammatory biomarkers, including neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), systemic immune-inflammation index, monocyte-to-lymphocyte ratio (MLR), and systemic inflammation response index. These values will be analysed in relation to the incidence of postoperative nausea and vomiting within the first 6 hours after pediatric orchiopexy. No experimental drug or device will be administered as part of the study; all procedures will be conducted within the scope of standard perioperative care.

Study summary

Orchiopexy is a common surgical procedure for the treatment of cryptorchidism in the pediatric population, with a high incidence of postoperative nausea and vomiting (PONV).

Recent evidence suggests that systemic inflammation may contribute to PONV pathogenesis, and preoperative inflammatory biomarkers such as NLR, PLR, SII, MLR, and SIRI could serve as predictive indicators.

This prospective observational study aims to evaluate the relationship between these biomarkers and PONV incidence in children undergoing orchiopexy.

Eligibility

Sex
ALL
Min age
1 Year
Max age
8 Years
Healthy volunteers
No
Inclusion Criteria: * Patients aged between 1 and 8 years * Patients with ASA physical status I-II * Patients scheduled for elective orchiopexy * Obtained written informed consent from parents/guardians Exclusion Criteria: * Patients younger than 1 year or older than 8 years * Patients with ASA physical status III or higher * Presence of acute infection signs * History of previous nausea or vomiting

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ankara Etlik City Hospital Altındağ Ankara Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07148063 on ClinicalTrials.gov ↗ ← All trials in Turkey