MULTIMODAL APPROACH IN THE DIAGNOSIS OF SEPTIC AKI
- Sponsor
- Ankara Etlik City Hospital
- Study ID
- NCT07472452
- Status
- Not Yet Recruiting
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Conditions
- Acute Kidney Injury
- Critical Illness
- Renal Resistive Index
- Sepsis
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Renal Resistive Index (RRI) Doppler Ultrasound — DIAGNOSTIC_TESTDoppler ultrasonography will measure RRI immediately after sepsis diagnosis (T0), at 24 hours (T24), and at 48 hours (T48).
- Urinary TIMP-2 and IGFBP-7 biomarkers — DIAGNOSTIC_TESTUrine samples for \[TIMP-2\]\*\[IGFBP-7\] biomarker measurement will be collected immediately after sepsis diagnosis (T0) and 24 hours later (T24).
Study Details
In recent studies, it has been reported that the renal resistance index is effective in detecting sepsis-related acute renal failure (SA-AKI) in the early period. Similarly, urinary biomarkers \[TIMP-2\]\*\[IGFBP-7\], released in response to tubular epithelial cell stress, have been reported to indicate the presence of acute renal injury (AKI) early on, before functional loss occurs (increased creatinine). This observational study aims to evaluate the renal resistance index and urinary biomarker variation in patients diagnosed with sepsis and to investigate their usefulness in the early detection of renal dysfunction that may develop after sepsis.
Key Dates
- First listed
- Mar 16, 2026
- Start date
- Mar 30, 2026
- Status verified
- Mar 2026
- Primary completion
- Jun 30, 2026
- Completion
- Jan 30, 2027
Study Design
- Enrollment
- 130 participants (estimated)
Arms
- Arm: Sepsis ICU CohortAdult patients (≥ 18 years of age) who are admitted to the intensive care unit with sepsis or who are diagnosed with sepsis during their admission and for whom bedside renal Doppler ultrasonography is feasible will be included in the study. Participants' Renal Resistive Index (RRI) measurements will be evaluated immediately after sepsis diagnosis (T0), at 24 hours (T24), and at 48 hours (T48). Urinary \[TIMP-2\]\*\[IGFBP-7\] measurements will be taken immediately after sepsis diagnosis (T0) and at 24 hours (T24). Clinical and laboratory data of the patients included in the study will be recorded for up to 72 hours after sepsis diagnosis. No treatment will be administered to the patients by the researchers; all medical care will be provided according to standard practice.
Primary Outcome Measure
Renal resistance index (RRI) [ Time Frame: Immediately after sepsis diagnosis (T0, baseline, first measurement) ]
Central Contacts
- Eda Macit Aydın, M.D., M.D.+90 312 797 00 00
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