Fatma Acil
Diyarbakır, Outside of the US, 21070, Turkey (Türkiye)
Location contact
Abdulkadir Yektaş, Prof.Dr.
CONTACT
Fatma Acil, M.D.
CONTACT
NCT Number: NCT07546448
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.
Trial opening soon.
Get Notified18 year–100 year
All sexes
Observational
Diyarbakır, Outside of the US, 21070, Turkey (Türkiye)
Abdulkadir Yektaş, Prof.Dr.
CONTACT
Fatma Acil, M.D.
CONTACT
This retrospective cohort study is designed to evaluate the association between serum electrolyte levels and the development of contrast-induced acute kidney injury (CI-AKI) in patients undergoing endovascular therapy (EVT) for acute ischemic stroke.
Endovascular treatment has become a standard of care for acute ischemic stroke; however, the use of iodinated contrast media carries a risk of nephrotoxicity. Contrast-induced acute kidney injury remains a clinically significant complication and is associated with prolonged hospitalization, increased healthcare costs, and higher mortality rates. Although several well-established risk factors for CI-AKI have been identified, including baseline renal dysfunction, diabetes mellitus, and contrast volume, the role of serum electrolyte imbalances has not been clearly defined.
Electrolyte disturbances may influence renal perfusion, tubular function, and systemic hemodynamics, potentially contributing to the pathophysiology of CI-AKI. Therefore, identifying electrolyte-related risk factors may help improve risk stratification and guide preventive strategies in high-risk populations.
In this study, patients who underwent EVT between 2018 and 2026 will be included. Prospectively collected clinical data will be analyzed retrospectively. Patients will be divided into two groups based on the development of CI-AKI, defined according to changes in serum creatinine levels following contrast exposure.
Comparative analyses will be performed between patients with and without CI-AKI to identify potential predictors. Multivariate regression analysis may be used to determine independent risk factors associated with CI-AKI development.
The findings of this study are expected to provide clinically relevant insights into the role of electrolyte balance in the development of CI-AKI and may contribute to improved peri-procedural risk assessment and patient management strategies in acute ischemic stroke populations undergoing endovascular therapy.
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Time frame: Within 48-72 hours after contrast exposure
CI-AKI will be identified based on post-procedural serum creatinine changes after contrast exposure according to established diagnostic criteria.
Time frame: Within 90 days after endovascular therapy
All-cause mortality occurring within 90 days after endovascular therapy in patients with and without contrast-induced acute kidney injury (CI-AKI).
Time frame: Within 90 days after endovascular therapy
Requirement for renal replacement therapy (hemodialysis) within 90 days after endovascular therapy in patients who developed contrast-induced acute kidney injury (CI-AKI)
Time frame: Baseline to 48-72 hours after endovascular therapy
Change in serum creatinine levels from baseline to post-procedural measurements following contrast exposure.
Time frame: Baseline (pre-procedural measurements)
Evaluation of the relationship between baseline serum electrolyte levels (sodium, potassium, chloride, calcium, magnesium, phosphate) and the development of contrast-induced acute kidney injury.
Time frame: Within 90 days after endovascular therapy
Total duration of hospitalization in days, compared between patients with and without CI-AKI.
Time frame: Baseline (pre-procedural measurements)
Association between inflammatory markers (e.g., C-reactive protein, procalcitonin) and the development of CI-AKI.
Time frame: Baseline to 48-72 hours after endovascular therapy
Change in estimated glomerular filtration rate (eGFR) from baseline to post-procedural measurements following contrast exposure
Contact information is provided by the study sponsor or research team.
Abdulkadir Yektaş, Prof.Dr.
CONTACT
Fatma Acil, M.D.
CONTACT
Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital
Other
The Impact of Serum Electrolyte Levels on the Risk of Contrast-Induced Nephropathy in Patients With Acute Ischemic Stroke Undergoing Endovascular Therapy
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05145283
Acute Ischemic Stroke, Acute Kidney Injury
Basel, Switzerland
View Trial DetailsNCT07013396
Acute Ischemic Stroke, Anterior Cerebral Artery Stroke
Richmond, Virginia, United States
View Trial DetailsNCT07682922
Acute Ischemic Stroke, Brain Diseases
Chongqing, Chongqing Municipality, China
View Trial DetailsNCT07672795
Acute Ischemic Stroke, Basilar Artery Occlusion
View Trial Details