"The effect of dynamic inflammatory changes and nutritional risk scores on mortality in intensive care patients aged 65 years and older"
NCT ID NCT07888010
First seen Oct 22, 2026 · Last updated Oct 22, 2026
Summary
"This prospective observational study aims to evaluate the prognostic value of dynamic changes in the serum uric acid-to-albumin ratio (UAR) measured on admission (Day 0) and on Day 3, along with mNUTRIC and PNI scores, regarding 28-day mortality in intensive care patients aged 65 and older."
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 224 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Nov 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients aged 65 and older who were admitted to the intensive care units of Ankara Etlik City Hospital and followed for at least 72 hours.
- Ages
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65 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Being 65 years of age or older * Having been followed up in the intensive care unit for at least 72 hours * Provision of written informed consent from the patient or their legal representative Exclusion Criteria: * Patients with terminal-stage malignancy * Chronic kidney disease of KDIGO stage 4 or higher * End-stage liver disease * Active hematological malignancy * Patients receiving immunosuppressive therapy * Patients with an active gout attack or using uric acid-lowering therapy
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Ankara Etlik City Hospital
Ankara, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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- Investigation of factors influencing outcomes in patients requiring ECMO and impella support, with special focus on their metabolic and thyroid hormone changes (Az ECMO és impella kezelést igénylő betegek kimenetelét befolyásoló tényezők vizsgálata, különös tekintettel metabolikus és pajzsmirigyhormon változásaikra)
- Ultrasound offers a window into stomach emptying for ICU patients
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