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Prospective randomized controlled study of CRRT hemofilters for the treatment of acute kidney injury (AKI)

Not Applicable
Conditions
Acute kidney injury (AKI)
Registration Number
JPRN-UMIN000016105
Lead Sponsor
Wakayama Medical University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
60
Inclusion Criteria

Not provided

Exclusion Criteria

- age less than 18 - pregnant women - chronic hemodialysis patients or patients who received RRT before randomization - end stage cancer patients

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
28-day mortality
Secondary Outcome Measures
NameTimeMethod
60-day mortality. Changes of SOFA score at 3 and 7 days after CRRT. Changes of plasma IL-6 levels at 1, 3, and 7 days after CRRT. Changes of lactate levels at 1, 3, and 7 days after CRRT. ICU free-days at Day 28. RRT free-days at Day 28. Progression to ESRD requiring maintenance hemodialysis. (subgroup analysis) septic AKI and non-septic AKI. with and without endotoxin removal hemoperfusion therapy.
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