Effects of hemoglobin levels on kidney injury after emergency surgery

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 observational study aims to evaluate how preoperative hemoglobin levels affect the development of acute kidney injury (AKI) in patients undergoing emergency non-cardiac surgery. Patients will be categorized into two groups based on whether they develop AKI postoperatively. The study will collect demographic data, blood counts, biochemistry, hemodynamic variables, and surgical characteristics to analyze the relationship between hemoglobin levels and AKI outcomes. The findings could clarify the role of hemoglobin optimization in preventing kidney complications in critically ill surgical patients.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients undergoing emergency non-cardiac surgery

Exclusion Criteria:

* Known renal failure
* Need for reoperation within 48 hours postoperatively
* Exit status within 48 hours postoperatively
* Known hematological disease
* Known kidney transplantation
* Urgent surgery planned due to urinary system related diseases
* Patients who did not accept to participate in the study

Where it's running

• Özgür Kömürcü
  Samsun, Turkey (Türkiye) Recruiting

Study contacts

• Study coordinator: özgür kömürcü, 1
• Email: zgrkom@gmail.com
• Phone: 90 5055273180

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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.