Preoperative blood inflammation markers to predict nausea after orchiopexy in children

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective observational study will enroll children aged 1–8 undergoing elective orchiopexy and record preoperative inflammatory markers including NLR, PLR, SII, MLR, and SIRI. Blood counts will be measured before surgery and patients will be monitored for postoperative nausea and vomiting during the immediate recovery period. Researchers will analyze whether baseline marker levels correlate with PONV incidence while excluding children with active infection, prior nausea/vomiting history, or ASA III+ status. The goal is to see if routine laboratory measures can identify higher-risk children for targeted prophylaxis.

Why it matters

Who can join: the full rules

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

Where it's running

• Ankara Etlik City Hospital
  Altındağ, Ankara, Turkey (Türkiye) Recruiting

Study contacts

• Study coordinator: Elif Şule Özdemir Sezgi
• Email: elifsule-91@hotmail.com
• Phone: 00905059209638

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.