RecruitingPhase 2ACTRN12625001227482

Response to frusemide in critically ill patients requiring dialysis

Frusemide stress test responsiveness in critically ill patients requiring continuous renal replacement therapy patients (FST-CRRT): a feasibility study


Sponsor

St Vincent's Hospital, Melbourne

Enrollment

40 participants

Start Date

Dec 11, 2024

Study Type

Interventional

Conditions

Summary

The administration of furosemide (a diuretic drug designed to increase production of urine) has been shown to predict a critically ill patient's requirement for dialysis (CRRT). This has been termed the frusemide stress test (FST). Critically ill patients often require dialysis in ICU for severe injury to the kidneys. There is a large amount of evidence around when to start, however there is little to guide clinicians on when the optimal time to stop dialysis is. This is important as whilst dialysis may be life saving, once the kidneys have started to recover it can result in harm. We aim to seek the proportion of patients who respond to the FST and identify whether a future randomised trial to aid clinicians in stopping dialysis at an appropriate time is feasible.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

When patients in the intensive care unit develop severe kidney injury, they often need continuous dialysis (a form of kidney replacement therapy called CRRT) to keep them alive. But knowing the right time to stop dialysis — once the kidneys start to recover — is tricky. Stopping too early can be harmful, but continuing dialysis longer than necessary can also cause problems. This study is exploring whether a simple test called the furosemide stress test (FST) — giving a dose of furosemide, a common diuretic, and measuring how much urine the patient produces in response — can help doctors judge when a patient's kidneys have recovered enough to stop dialysis. This early-phase study will assess what proportion of ICU patients respond to the test, and whether a larger future trial to guide this decision is feasible. You may be eligible if you are 18 or older, are in the ICU receiving continuous dialysis for kidney injury (or have had it paused for under 12 hours), have been on dialysis for more than 24 hours, and your vital signs and fluid balance are stable. People with a known allergy to furosemide, end-stage kidney disease, or who are pregnant or breastfeeding are not eligible.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

The administration of a single dose of intravenous frusemide will be administered at 1mg/kg (or 1.5mg/kg if received frusemide in the past seven days). The intervention will be administered as soon as

The administration of a single dose of intravenous frusemide will be administered at 1mg/kg (or 1.5mg/kg if received frusemide in the past seven days). The intervention will be administered as soon as practically possible once all inclusion criteria are met and with agreement from the treating intensivist. Medication charts will be reviewed to confirm administration.


Locations(2)

St Vincent's Hospital (Melbourne) Ltd - Fitzroy

VIC, Australia

Austin Health - Austin Hospital - Heidelberg

VIC, Australia

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ACTRN12625001227482


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