Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06446739

LoW Dose-Intensity vs. Standard Dose-Intensity Continuous Renal Replacement Therapy in Critically Ill Patients (WISDOM): A Pilot Randomized Trial

Led by University of Alberta · Updated on 2026-04-28

100

Participants Needed

9

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of different dose-intensities of continuous renal replacement therapy (CRRT) in critically ill patients with acute kidney injury (AKI) who require dialysis in the intensive care unit. The study aims to determine whether a lower CRRT dose-intensity is as effective as the current standard dose, with the hope that a lower dose may improve kidney recovery, shorten dialysis duration, and reduce costs and nursing workload. This trial is a pilot randomized study designed to generate high-quality evidence to guide future clinical practice. Participants will be randomly assigned to one of two groups: the intervention group will receive a low dose-intensity CRRT of 10-15 mL/kg/hr, while the control group will receive the standard dose-intensity of 25-30 mL/kg/hr, as recommended by current guidelines. Treatments will be delivered continuously while patients require CRRT in the intensive care unit. The trial focuses on comparing these two dosing strategies during the CRRT period. During the study, researchers will monitor the delivered CRRT dose-intensity for about one month and assess feasibility measures such as consent rate, recruitment rate, and adherence to the assigned dose over 90 days. They will also evaluate patient outcomes related to CRRT duration and kidney recovery. Participants or their representatives will provide informed consent, and safety and compliance with the study protocol will be closely followed throughout the trial period.

CONDITIONS

Brief Title

LoW Dose-Intensity vs. Standard Dose-Intensity COntinuous Renal ReplaceMent Therapy in Critically Ill Patients (WISDOM)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Weight at least 55 kilograms
  • Plan to start CRRT or started CRRT within the last 24 hours for acute kidney injury
  • Expected to survive and receive CRRT for at least 48 hours
  • Able to provide informed consent or have a representative provide consent unless deferred consent is approved
Not Eligible

You will not qualify if you...

  • Need for sustained higher dose-intensity CRRT as determined by attending clinicians
  • End-stage kidney disease receiving maintenance dialysis
  • Receiving any renal replacement therapy for acute kidney injury during the current hospitalization
  • Unable to comply with study protocol requirements

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Until kidney recovery or liberation from CRRT

Participants receive continuous renal replacement therapy (CRRT) at either a low dose-intensity or standard dose-intensity while being critically ill with acute kidney injury.

Continuous therapy in the intensive care unit

Follow-up

Duration - Up to 90 days

Participants are monitored for up to 90 days to assess kidney recovery, duration of CRRT, and adherence to prescribed dose-intensity.

Follow-up assessments as per clinical care

Trial Site Locations

Total: 9 locations

1

Mayo Clinic

Rochester, Minnesota, United States, 55905

Actively Recruiting

2

University of Alberta Hospital

Edmonton, Alberta, Canada, T6G 2B7

Actively Recruiting

3

Grey Nuns Hospital

Edmonton, Alberta, Canada

Actively Recruiting

4

Sturgeon Community Hospital

St. Albert, Alberta, Canada, T8N 6C4

Actively Recruiting

5

Hamilton General Hospital

Hamilton, Ontario, Canada

Actively Recruiting

6

Sunnybrook Health Sciences Centre

North York, Ontario, Canada, M4N 3M5

Actively Recruiting

7

St Michael's Hospital

Toronto, Ontario, Canada

Actively Recruiting

8

Regina General Hospital/Saskatchewan Health Authority

Regina, Saskatchewan, Canada

Actively Recruiting

9

Guy's & St Thomas' Hospitals

London, United Kingdom, SE1 9RT

Actively Recruiting

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Research Team

S

Sean M Bagshaw, MD

E

Ellen Morrison, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Proceedings of the University of Alabama at Birmingham Continuous Renal Replacement Therapy Academy (2023-2024): Managing De-Escalation of Acute Renal Replacement Therapy and Optimizing Drug Dosing during Renal Replacement Therapy Transitions.

William Beaubien-Souligny, Melissa Thompson Bastin, J Pedro Teixeira...

https://pubmed.ncbi.nlm.nih.gov/40779331