Status:

RECRUITING

Efficacy and Safety of Citrate Anticoagulation in CRRT for Patients With Liver Failure/DysfuncTION, the CAUTION Trial! A Retrospective Study on Etiology of Liver Failure and Their Complications

Lead Sponsor:

University Hospital, Antwerp

Conditions:

Liver Failure

AKI - Acute Kidney Injury

Eligibility:

All Genders

18+ years

Brief Summary

Study design A retrospective cohort study will be conducted to compare the efficacy and safety of citrate anticoagulation in CRRT among patients with liver failure/dysfunction and severe shock. Objec...

Detailed Description

Continuous renal replacement therapy (CRRT) is a crucial intervention for managing acute kidney injury (AKI) in critically ill patients. Citrate anticoagulation has become a preferred method in CRRT d...

Eligibility Criteria

Inclusion

  • Critically ill patients diagnosed with AKI requiring CRRT. Caution Protocol V1.0 24-07-2024
  • Documented liver failure or significant liver dysfunction (e.g., elevated liver enzymes, bilirubin levels, or clinical diagnosis of liver failure) and clincal diagnosis of shock (NE of 0.25 μg/kg/min and or association of second vasopressor).
  • Age ≥ 18 years.

Exclusion

  • NA

Key Trial Info

Start Date :

September 30 2024

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

December 31 2025

Estimated Enrollment :

100 Patients enrolled

Trial Details

Trial ID

NCT06908746

Start Date

September 30 2024

End Date

December 31 2025

Last Update

April 3 2025

Active Locations (1)

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Antwerp University Hospital

Edegem, Antwerp, Belgium, 2650