The Effect of Standard vs. Shorter Filter Lifespan During Continuous Renal Replacement Therapy

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversität Münster

About this trial

This study aims to investigate shorter vs. standard filter lifespans in critically ill patients receiving continuous renal replacement therapy (CRRT) for acute kidney injury (AKI). The aim of this trial is to reliably implement,scheduled filter changes and to investigate whether shorter filter lifetime is associated with a lower incidence in rate of new infections.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult ≥ 18 years

Critically ill patients with severe AKI consistent with KDIGO stage 3 and an absolute indication for CRRT

Written consent form from the patient or legal representative or authorized representative or emergency inclusion

Disqualifiers

End-stage kidney disease or chronic dialysis dependence

Chronic kidney disease with eGFR<20ml/min/1.73 m²

Prior kidney transplant

Prior renal replacement therapy during the index admission before randomization

Trial design

Design model

Parallel

Treatments tested in this trial

  • time span of filter change

    Other intervention

    The time span of the filter change during continuous renal replacement therapy will be specified

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Early filter changeExperimental treatment 1 intervention
Group B: Standard of Care filter changeActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Mean filter lifespan per patient

Comparison of mean filter lifespans between study groups

Time frame
From start of CRRT to end of CRRT or at day 30 after randomization, whatever occurs first
2

Protocol adherence as documented filter change within the specified period

Proportion of protocol adherent patients, defined as patients with mean filter lifespan within the pre-specified time window in each arm (intervention group: 36±3hours; control group: 48-72hours

Time frame
From start of CRRT to end of CRRT or at day 30 after randomization, whatever occurs first

Secondary outcomes

1

New intensive care unit (ICU)-associated acquired infection up to day 30

Rate of new ICU-acquired infections, defined as new infection in patients with pre-existing infection but with another pathogen than baseline or without baseline infection. All infections need to be culture proven. Only the first infection per patient will be considered

Time frame
From start of CRRT to end of CRRT or at day 30 after randomization, whatever occurs first

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: