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Study identifier: NCT06834633 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Nephroprotection in Severe Trauma Patients With Kidney Stress

Condition: Trauma; Complications  ·  Sponsor: Hospices Civils de Lyon

PhaseNA
Planned participants523
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Acute Kidney Injury (AKI) occurs in 24% of trauma patients, and is even more common in those with severe trauma. It is a major contributor to morbidity and mortality in trauma. Diagnosis of AKI is based on elevated serum creatinine and decreased urine output, two functional markers already indicating the presence of a significant kidney function impairment. Earlier detection of kidney stress, at a preclinical stage when cellular modifications are still reversible, could reduce the occurrence of AKI episodes if nephroprotective measures are rapidly implemented. Several randomized controlled trials have shown that early implementation of such a nephroprotection bundle-of-care in patients at risk of AKI after major surgery reduces the incidence of severe AKI within 72 hours. Although its use is supported by international guidelines, this nephroprotection bundle-of-care is rarely implemented in its totality, due to the significant financial and human resources required for its full implementation. The Nephrocheck® (NC) test is a urine test for which a result \> 0.3 is predictive of AKI development. It might enable early identification of trauma patients at risk of AKI, so that implementation of the nephroprotection bundle-of-care could be targeted solely at those high-risk patients. Thus, the investigators hypothesize that in a population of severe trauma patients (ISS score\>15) at risk of AKI (defined by a NC on Intensive Care Unit (ICU) admission \> 0.3), early implementati…

This description comes directly from the study's public registry record.

Talk to the study team

Céline MONARD  ·  04 72 11 13 27  ·  celine.monard@chu-lyon.fr

Karine POYAU  ·  04 72 11 53 81  ·  karine.poyau@chu-lyon.fr

Always discuss trial participation with your own doctor first.

Locations (6)

Centre Hospitalier universitaire Estaing, Service anesthésie-réanimationClermont-Ferrand, FranceNot Yet Recruiting
Centre hospitaler Annecy Genevois, Service de réanimationÉpagny, FranceNot Yet Recruiting
Centre hospitalier universitaire de Grenoble Alpes, Pôle anesthésie-réanimationLa Tronche, FranceNot Yet Recruiting
Hospices Civils de Lyon, Hôpital Edouard Herriot, Service d'anesthésie-réanimationLyon, FranceRecruiting
Hospices Civils de Lyon, Hôpital Lyon-Sud, Service d'anesthésie-réanimationPierre-Bénite, FranceRecruiting
Centre hospitalier universitaire de Saint Etienne, Hôpital Bellevue, Service anesthésie-réanimationSaint-Etienne, FranceNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT06834633