Recruitment

Recruitment Status
Completed
Estimated Enrollment
20

Inclusion Criterias

Written informed consent from the patient or legal representative
Critically ill patients requiring CRRT for AKI (RIFLE criteria)
Written informed consent from the patient or legal representative
Critically ill patients requiring CRRT for AKI (RIFLE criteria)

Exclusion Criterias

pre-existing chronic renal insufficiency requiring dialysis
Pregnancy
severe or shock-related hepatitis
...
pre-existing chronic renal insufficiency requiring dialysis
Pregnancy
severe or shock-related hepatitis
liver cirrhosis Child-Pugh C
chronic immunosuppression

Summary

Conditions
  • Acute Kidney Injury
  • Critically Ill
Type
Interventional
Design
  • Allocation: Randomized
  • Intervention Model: Parallel Assignment
  • Masking: None (Open Label)
  • Primary Purpose: Supportive Care

Participation Requirements

Age
Younger than 125 years
Gender
Both males and females

Inclusion Criterias

Written informed consent from the patient or legal representative
Critically ill patients requiring CRRT for AKI (RIFLE criteria)
Written informed consent from the patient or legal representative
Critically ill patients requiring CRRT for AKI (RIFLE criteria)

Exclusion Criterias

pre-existing chronic renal insufficiency requiring dialysis
Pregnancy
severe or shock-related hepatitis
...
pre-existing chronic renal insufficiency requiring dialysis
Pregnancy
severe or shock-related hepatitis
liver cirrhosis Child-Pugh C
chronic immunosuppression

Locations

Genk, Limburg, 3600
Genk, Limburg, 3600

Tracking Information

NCT #
NCT02194569
Collaborators
Not Provided
Investigators
  • Principal Investigator: Willem Boer, MD Ziekenhuis Oost-Limburg
  • Willem Boer, MD Ziekenhuis Oost-Limburg