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French AKI Registry (FAKIR): A Multicenter Study on the In-Hospital Management and Outcomes of Severe Acute Kidney Injury in Nephrology Units

U

University Hospital, Strasbourg, France

Status

Not yet enrolling

Conditions

Cardiorenal Syndrome
Acute Kidney Injury
Kidney Failure Chronic
Hospitalizations
Renal Replacement Therapies

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Acute Kidney Injury (AKI) is a common and serious condition in hospitalized patients, especially when it reaches stages 2 or 3 according to the KDIGO classification. These severe forms are associated with high mortality, a risk of progression to chronic kidney disease (CKD), and frequent cardiovascular complications. However, current data on how nephrologists manage these patients during hospitalization-and how these practices influence long-term outcomes-are limited and heterogeneous.

The FAKIR study (French AKI Registry) is a prospective, multicenter, non-interventional observational study designed to describe the clinical management of patients admitted to nephrology departments for AKI stage 2 or 3 and to assess their renal and cardiovascular outcomes up to one year. The study hypothesizes that better characterization of in-hospital practices and patient trajectories will help identify predictors of renal recovery, progression to end-stage renal disease, and major cardiovascular events.

Patients will be followed during hospitalization and at 3, 6, and 12 months to assess renal function, mortality, cardiovascular events, and rehospitalizations. This registry aims to provide real-life, multicenter data to support future guidelines and the development of structured post-AKI care pathways.

Enrollment

750 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥ 18 years at admission
  • Hospitalized in a nephrology ward (standard or intensive nephrology care unit)
  • Diagnosis of acute kidney injury (AKI) stage 2 or 3 according to KDIGO criteria at the time of admission
  • Availability of follow-up data at 3 months (clinical or laboratory)

Exclusion criteria

  • AKI stage 1 only
  • AKI acquired outside the nephrology department without subsequent transfer to nephrology
  • Hospitalized for another reason without documented AKI stage 2 or 3
  • Refusal or opposition to data reuse for research purposes
  • Under legal protection (guardianship or trusteeship) without a representative to provide non-opposition
  • Incomplete medical records preventing collection of required baseline data

Trial design

750 participants in 1 patient group

AKI KDIGO 2-3 Nephrology Patients
Description:
This cohort includes adult patients (≥18 years old) hospitalized in nephrology wards (including conventional units and nephrology intensive care) for acute kidney injury (AKI) classified as KDIGO stage 2 or 3 at admission. Patients with AKI acquired outside nephrology or limited to stage 1 are excluded. Clinical data will be collected during hospitalization and follow-up visits at 3, 6, and 12 months to assess renal recovery, progression to chronic kidney disease, major cardiovascular events, and mortality. This group represents real-life management of severe AKI in nephrology units across multiple centers.

Trial contacts and locations

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Central trial contact

Mallaury Vervaeke

Data sourced from clinicaltrials.gov

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