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NCT06652100: EPACRA-AKI

Establishment of ProNephro AKI (NGAL) Cut Off Value for Risk Assessment of Moderate to Severe Acute Kidney Injury in Adults

Active, enrolled Last updated 19 November 2025
What this trial tests

trial testing ProNephro AKI (NGAL) in Acute Kidney Injury in 800 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
28 October 2024
Primary endpoint
30 January 2026
31 January 2026

Quick facts

Lead sponsorBioPorto Diagnostics
StatusActive, enrolled
Study typeOBSERVATIONAL
Enrollment800
Start date28 October 2024
Primary completion30 January 2026
Estimated completion31 January 2026
Sites12 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

BioPorto Diagnostics

Who can join

22 and older, any sex, with Acute Kidney Injury. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this research is to collect blood and urine from adult patients admitted to an intensive care unit. This is to assess the performance of the ProNephro AKI (NGAL) assay (lab test) as an aid to identify patients at risk for acute kidney injury.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Clinical Implementation of Urinary Neutrophil Gelatinase-Associated Lipocalin Testing for Diagnosing Acute Kidney Injury in an Academic Tertiary Care Medical Centre.
    Strader M, Imran S, Tariq A, Fraser C, et al · · 2025 · cited 2× · PMID 40802457 · DOI 10.34067/kid.0000000887

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Other recruiting trials for Acute Kidney Injury

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06652100.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing