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Clinical Trials in Turkey / NCT07546448
Starting soon Observational

Serum Electrolytes and Contrast-Induced Nephropathy in Acute Ischemic Stroke Patients Undergoing Endovascular Treatment

NCT07546448 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-04-20
Last updated
2026-04-22

Condition(s) studied

Acute Ischemic StrokeContrast-induced NephropathyAcute Kidney Injury

Investigational drug(s) / intervention(s)

No intervention (observational cohort study)

No intervention (observational cohort study): No experimental or therapeutic intervention was assigned. This observational retrospective cohort study evaluated patients undergoing endovascular therapy for acute ischemic stroke, who were subsequently categorized based on the presence or absence of contrast-induced acute kidney injury (CI-AKI). The study analyzed demographic, clinical, laboratory (including serum electrolyte levels) and procedural variables to identify potential risk factors associated with CI-AKI development.

Study summary

This study aims to evaluate the relationship between serum electrolyte levels and the development of contrast-induced acute kidney injury (CI-AKI) in patients with acute ischemic stroke undergoing endovascular therapy (EVT).

Contrast-induced nephropathy remains a significant complication associated with endovascular procedures and is linked to increased morbidity and mortality. While several risk factors have been identified, the role of serum electrolyte imbalances in the development of CI-AKI has not been fully elucidated.

In this retrospective cohort study, patients treated with EVT between 2018 and 2026 will be analyzed. Patients will be classified based on the presence or absence of CI-AKI according to changes in serum creatinine levels. Demographic data, comorbidities, laboratory parameters-including serum electrolytes-and procedural variables will be compared between groups.

The primary objective is to determine whether serum electrolyte levels are associated with the risk of CI-AKI. Secondary objectives include evaluating 90-day mortality and dialysis dependency in patients who develop CI-AKI.

Eligibility

Sex
ALL
Min age
18 Years
Max age
100 Years
Healthy volunteers
No
Inclusion Criteria: * Adults aged 18 years or older * Patients diagnosed with acute ischemic stroke * Patients who underwent endovascular therapy for acute ischemic stroke between 2018 and 2026 * Patients with a baseline NIHSS score of 6 or higher * Patients who received iodinated contrast medium during the endovascular procedure * Patients managed under general anesthesia * Patients with available pre-procedural and post-procedural serum creatinine measurements sufficient to assess contrast-induced acute kidney injury Exclusion Criteria: * Age younger than 18 years * Pre-existing acute kidney injury or chronic kidney disease meeting KDIGO stage 1-3 before endovascular therapy * APACHE score greater than 25 at the time of the procedure * Known allergy or hypersensitivity to iodinated contrast media * Exposure to iodinated contrast media within the previous 2 weeks * Use of nephrotoxic medications within the previous 2 weeks * History of myocardial infarction or previous stroke * Use of vasopressor/inotropic agents such as dopamine at the time of the procedure * Systemic steroid use at the time of the procedure * Incomplete medical records or missing laboratory data required for evaluation of CI-AKI

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Fatma Acil Diyarbakır Outside of the US

More Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital trials in Turkey

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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 NCT07546448 on ClinicalTrials.gov ↗ ← All trials in Turkey