NCT07586059

Brief Summary

This large national cohort study, including over 500,000 patients, where around 5% are treated with continuous renal replacement therapy (CRRT) , aims to evaluate the association between time to initiation of CRRT and intensive care unit (ICU) length of stay (LOS).

Trial Health

65
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
500,000

participants targeted

Target at P75+ for all trials

Timeline
5mo left

Started Aug 2026

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 18, 2025

Completed
5 months until next milestone

First Posted

Study publicly available on registry

May 14, 2026

Completed
3 months until next milestone

Study Start

First participant enrolled

August 1, 2026

Expected
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

May 20, 2026

Status Verified

May 1, 2026

Enrollment Period

5 months

First QC Date

December 18, 2025

Last Update Submit

May 18, 2026

Conditions

Keywords

AKICRRTCKRTCritical IllnessIntensive care

Outcome Measures

Primary Outcomes (1)

  • Intensive care unit (ICU) length of stay (LOS) measured in hours

    Hours from baseline, i.e. ICU admission (time=0) to ICU discharge (time=0+hours in ICU)

    ICU LOS during the study period, from admission to discharge, average 168 hours (one week)

Secondary Outcomes (2)

  • Mortality

    ONE-YEAR Mortality post admission

  • Mechanical ventilation

    Time on mechanical ventilation during the study period, average one week, but up to ICU discharge

Interventions

We are evaluting early vs late initiation of CRRT

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

All adult critically ill patients in Swedish ICUs from 2010-2023, with- and without the need of CRRT forms this cohort. Within the cohort, a nested case-control type of study can be performed. Two groups: Group 1: Patients with CRRT initiation time less than 30 hours (early CRRT) Group 2: Patients with CRRT initiation time 30 hours or more (late CRRT)

You may qualify if:

  • Patients with critical illness
  • Admitted to Swedish ICUs from 2010-2023
  • Adult (18 years or older)

You may not qualify if:

  • \*Patients under 18 years of age

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Acute Kidney InjuryCritical Illness

Interventions

Continuous Renal Replacement Therapy

Condition Hierarchy (Ancestors)

Renal InsufficiencyKidney DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Renal Replacement TherapyTherapeuticsExtracorporeal CirculationSurgical Procedures, Operative

Study Officials

  • Max Bell, MD, PhD

    Karolinska University Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
MD, PhD, senior lecturer, associate professor

Study Record Dates

First Submitted

December 18, 2025

First Posted

May 14, 2026

Study Start (Estimated)

August 1, 2026

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

May 20, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Swedish law prohibits IPD sharing using extracted quality register data, when this has not been stated in the primary ethics application. However, other researchers can theoretically apply for data extraction from the Swedish Intensive Care Register.