Continuous Renal Replacement Therapy, Impact on Intensive Care Unit Length of Stay
CIILOS
CIILOS - Continuous Renal Replacement Therapy, Impact on Intensive Care Unit Length of Stay
1 other identifier
observational
500,000
0 countries
N/A
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2026
Shorter than P25 for all trials
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
CompletedFirst Posted
Study publicly available on registry
May 14, 2026
CompletedStudy Start
First participant enrolled
August 1, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2026
Study Completion
Last participant's last visit for all outcomes
December 31, 2026
May 20, 2026
May 1, 2026
5 months
December 18, 2025
May 18, 2026
Conditions
Keywords
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
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
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Max Bell, MD, PhD
Karolinska University Hospital
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.