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Acute Kidney InjuryCRRTinfUKNCT07903519

Effect of Filter Lifespan in CRRT on New Infections in Critically Ill Patients With AKI

An observational study of Acute Kidney Injury, run by Guy's and St Thomas' NHS Foundation Trust at 1 site in United Kingdom.

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 observational study aims to explore the factors that influence the risk of new infections in critically ill patients with acute kidney injury (AKI) requiring continuous renal replacement therapy (CRRT) in the UK. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Acute Kidney Injury
How many people
630 participants
Where
1 siteUnited Kingdom
Study dates
1 Nov 2026to 1 Jun 2028
Phase
Observational
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

Study population: critically ill adult patients with AKI requiring CRRT

Who may be able to join

  • age ≥ 18 years
  • critically ill patients with AKI in whom CRRT is planned

Who cannot join

  • chronic kidney disease with eGFR<30ml/min/1.73m2
  • Chronic dialysis dependency
  • kidney transplant
  • known (Glomerulo-) nephritis, interstitial nephritis, vasculitis
  • known to be on immunosuppression, including Methotrexate, Cyclosporine, Antibody immunosuppression (e.g., rituximab, infliximab), Glucocorticoid as long-term medication at a dose above the cushing threshold
  • known chronic inflammatory diseases (e.g. arthritis, HIV with a CD4 count of < 0.05 x 10E/l, chronic hepatitis)
  • participation in an interventional trial within the last 3 months investigating a drug that affects kidney function

Trial locations and contacts

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

Marlies Ostermann, PhD contact

+447742514213

m.ostermann@nhs.net

Gillian Radcliffe contact

00442071883036

gill.radcliffe@nhs.net

United Kingdom1 site
  • Guy's & St Thomas' Hospital

    London, Greater London, SE1 7EH

    Marlies Ostermann, PhD, 07742514213, Marlies.Ostermann@gstt.nhs.uk

Other trials in United Kingdom

About this study

Official title: The Effect of Filter Lifespan in Continuous Renal Replacement Therapy on the Rate of New Infections in Critically Ill Patients With AKI: a Prospective Observational Study

This observational study aims to explore the factors that influence the risk of new infections in critically ill patients with acute kidney injury (AKI) requiring continuous renal replacement therapy (CRRT) in the UK.

Read the detailed description

Acute kidney injury (AKI) is a potentially life threatening condition which affects 1 in 2 patients in the Intensive Care Unit (ICU). Patients often need renal replacement therapy (RRT). A secondary analysis of a RCT showed an association between circuit life and risk of infections.

The purpose of this study is to investigate the specific factors that influence the risk of new infections in critically ill patients with AKI requiring continuous renal replacement therapy (CRRT) in the UK and whether longer filter life is indeed a contributing factor.

Keywords
acute kidney injury, renal replacement therapy
Medical subject headings
Acute Kidney Injury

What participants receive

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

Study groups in NCT07903519
Study groupRoleWhat they receive
patients with AKItreated with CRRT

What is being measured

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

  1. number of new infections

    the number of new infections since start of CRRT, defined as new infections after initiation of CRRT

    Measured: up to day 28

Secondary outcomes (3)
  1. Renal and survival outcomes

    1. Days on renal replacement therapy (RRT) from start of CRRT until day 28

    Measured: 28 days

  2. Duration of mechanical ventilation from start of CRRT

    days on mechanical ventilation

    Measured: day 28

  3. hospital length of stay

    days in hospital

    Measured: day 60

Timeline

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

  1. First posted29 Oct 2026
  2. Study start1 Nov 2026 (estimated)
  3. Primary completion31 Dec 2027 (estimated)
  4. Study completion1 Jun 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
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
630 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07903519
Sponsor's protocol ID
CRRTinfUK
Acronym
CRRTinfUK
Status last verified
Sep 2026
First submitted
19 Sep 2025
Last updated
29 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Acute Kidney Injury, run by Guy's and St Thomas' NHS Foundation Trust at 1 site in United Kingdom.

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 2 inclusion and 7 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 29 Oct 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 United Kingdom. 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 Marlies Ostermann, PhD (+447742514213, m.ostermann@nhs.net), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

number of new infections (time frame: up to day 28). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 29 Oct 2026.

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