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Acute Kidney InjurySPECIALNCT07630220

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

A study testing time span of filter change in people with Acute Kidney Injury, run by Universität Münster at 1 site in Germany.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

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). Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Acute Kidney Injury
What is being tested?
time span of filter change
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteGermany
Study dates
Jun 2026to Jun 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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

Who cannot join

  • 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
  • Glomerulonephritis, interstitial nephritis, vasculitis
  • Patients on immunosuppression (above the cushing threshold)
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  • Patients with chronic inflammatory diseases (e.g. arthritis, HIV with a CD4 count of < 0.05 x 10E/l)
  • Do-not resuscitate order
  • Persons with any kind of dependency on the investigator or employed by the sponsor
  • Patients participating in an interventional study involving measures to influence the immune system

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Alexander Zarbock, MD contact

+49-251-8347255

zarbock@uni-muenster.de

Germany1 site
  • University Hospital Münster

    Münster, 48149

Other trials in Germany

About this study

Official title: The Effect of Standard vs. Shorter Filter Lifespan During Continuous Renal Replacement Therapy in Critically Ill Patients With Acute Kidney Injury - a Feasibility Randomized Controlled 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.

Read the detailed description

Own data of patients under standard care indicated that a longer filter lifetime in CRRT is associated with an increased rate of new infections.

The aim of this study is to demonstrate that a protocolized filter-change strategy can be reliably implemented in critically ill patients and a high protocol adherence can be achieved.

The secondary aim is to investigate whether a shorter filter-change strategy is be associated with a lower incidence of newly acquired infections.

Being tested
time span of filter change
Keywords
Continuous Renal Replacement Therapy (CRRT), Infection, filter change, critical illness
Medical subject headings
Acute Kidney Injury, Infections, Critical Illness

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • time span of filter changeOther

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

Study groups in NCT07630220
Study groupRoleWhat they receive
Early filter changeExperimentalScheduled filter change during continuous renal replacement therapy at 36 ± 3 hours.
Receives: Other: time span of filter change
Standard of Care filter changeActive comparatorStandard of care with scheduled filter change during continuous renal replacement therapy at 72 hours.
Receives: Other: time span of filter change

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Mean filter lifespan per patient

    Comparison of mean filter lifespans between study groups

    Measured: 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

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

Secondary outcomes (1)
  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

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

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Jun 2026
  2. Study startJun 2026 (estimated)
  3. Primary completionJun 2028 (estimated)
  4. Study completionJun 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07630220
Sponsor's protocol ID
AnIt26-02
Other IDs
DRKS00039623
Acronym
SPECIAL
Status last verified
May 2026
First submitted
1 Jun 2026
Last updated
15 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Gerss J, Meersch M, Kindgen-Milles D, Brandenburger T, Willam C, Kellum JA, Zarbock A. The Effect of Filter Lifespan during Continuous Renal Replacement Therapy in Critically Ill Patients with Acute Kidney Injury on the Rate of New-Onset Infection: Analysis from the RICH Randomized Controlled Trial. Am J Respir Crit Care Med. 2022 Aug 15;206(4):511-514. doi: 10.1164/rccm.202201-0063LE. No abstract available.

    PubMed 35549654
  • Zarbock A, Kullmar M, Kindgen-Milles D, Wempe C, Gerss J, Brandenburger T, Dimski T, Tyczynski B, Jahn M, Mulling N, Mehrlander M, Rosenberger P, Marx G, Simon TP, Jaschinski U, Deetjen P, Putensen C, Schewe JC, Kluge S, Jarczak D, Slowinski T, Bodenstein M, Meybohm P, Wirtz S, Moerer O, Kortgen A, Simon P, Bagshaw SM, Kellum JA, Meersch M; RICH Investigators and the Sepnet Trial Group. Effect of Regional Citrate Anticoagulation vs Systemic Heparin Anticoagulation During Continuous Kidney Replacement Therapy on Dialysis Filter Life Span and Mortality Among Critically Ill Patients With Acute Kidney Injury: A Randomized Clinical Trial. JAMA. 2020 Oct 27;324(16):1629-1639. doi: 10.1001/jama.2020.18618.

    PubMed 33095849

Questions about this trial

What is this clinical trial studying?

A study testing time span of filter change in people with Acute Kidney Injury, run by Universität Münster at 1 site in Germany.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 15 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Alexander Zarbock, MD (+49-251-8347255, zarbock@uni-muenster.de), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Mean filter lifespan per patient (time frame: From start of CRRT to end of CRRT or at day 30 after randomization, whatever occurs first). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07630220, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Jun 2026.

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