Nephroprotective Measures in Critically Ill Patients With Moderate/Severe Acute Kidney Injury
Condition(s) studied
Investigational drug(s) / intervention(s)
Nephroprotective measures: Due to the observational design of the study, no study specific interventions are performed. The treatment of the patients is completely guided by the responsible physicians.
Study summary
This study investigates to which extent recommended nephroprotective measures are implemented in critically ill patients with moderate or severe acute kidney injury.
Eligibility
Primary outcome measure(s)
- Rate of patients in whom "Kidney Disease: Improving Global Outcomes (KDIGO)" guideline recommendations are successfully implemented for 48 hours, following the onset of moderate/ severe AKI (defined by KDIGO criteria) — 60 hours after onset of moderate/severe AKI
Trial sites (3)
| Facility | City | Region | Status |
|---|---|---|---|
| Universitätsklinik Innsbruck | Innsbruck | Austria | Recruiting |
| University Hospital Münster; Department of Anesthesiology, Intensive Care Medicine and Pain Medicine | Münster | Germany | Recruiting |
| Radboud University medical cener | Nijmegen | Netherlands | Recruiting |
Other trials for the same condition
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 NCT06472999 on ClinicalTrials.gov ↗ ← All trials in the Netherlands