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Effect of a Furosemide Stress Test-Guided Strategy on Liberation From Continuous Renal Replacement Therapy in Critically Ill Patients With Acute Kidney Injury

Effect of a Furosemide Stress Test-Guided Strategy on Liberation From Continuous Renal Replacement Therapy in Critically Ill Patients With Acute Kidney Injury (FST-LIBERATE)

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06229990
Acronym
FST-LIBERATE
Enrollment
88
Registered
2024-01-29
Start date
2024-01-01
Completion date
2028-12-31
Last updated
2026-10-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Kidney Injury

Keywords

Acute kidney injury, Continuous renal replacement therapy, Furosemide stress test, Critical care, CRRT

Brief summary

Currently, continuous renal replacement therapy (CRRT) is the main modality for renal support in critically ill patients with hemodynamic instability. Most studies have investigated the timing of RRT initiation. However, prolonged CRRT demonstrated the association of many unexpected events, such as catheter-related complications, catheter-related blood stream infection, hypotension, hypothermia, tachycardia, and atrial fibrillation. Up to now, there is a lack of evidence regarding the timing of withholding CRRT. The furosemide stress test (FST) is a tool that is easy to use and has more availability. The investigators aimed to apply FST to evaluate renal recovery compared with standard treatment in critically ill patients undergoing CRRT.

Interventions

After taking furosemide at 1.5 mg/kg intravenously, if the urine output exceeds 200 mL within 2 hours, the patients are going to withhold CRRT. But if there is no response, the titration of furosemide to 2.5 mg/kg and 3.5 mg/kg every 6 hours is scheduled according to the urine output \>200 mL in 2 hours (not exceeding 250 mg).

Sponsors

Chiang Mai University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult 18 year of age or older * Acute kidney injury (AKI) stage 3 according to Kidney Disease Improving Global Outcomes (KDIGO) classification with oliguria (urine \<400 ml/day) * Initiate CRRT in ICU (medical ICU, surgical ICU, cardiac care unit) for at least 48 hours (time for initiation and modality of CRRT can adjust by clinician)

Exclusion criteria

* Use any inotropic drug (norepinephrine, epinephrine, dopamine, dobutamine) * Serum K \<3.5 or \>5 mmol/L * Arterial potential of Hydrogen (pH) \<7.3 * Serum bicarbonate (HCO3) \<15 mmol/L * Urine volume ≥2,300 mL/day * Previous chronic kidney disease (CKD) stage 5 or estimated glomerular filtration rate (eGFR) \<15 mL/min/1.73 m2 * Previous RRT within 14 days * Kidney transplantation * Obstructive etiology for AKI * Toxin/drug that necessitates RRT * Allergy to furosemide * Moribund with expected death within 24 hours * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Successful liberation from CRRT7 daysDiscontinuation of CRRT without reinitiation of any RRT modality within 7 days after CRRT discontinuation

Secondary

MeasureTime frameDescription
Urine output7 daysUrine output after each FST and during the first 7 days following randomization
Fluid balance7 daysFluid balance after each FST and during the first 7 days following randomization
CRRT reinitiation7 daysNumber of patients who need to restart CRRT
Total duration of RRTThrough study completion, an average of 90 daysIncluding first day of CRRT until last session of RRT
Ventilator-free dayThrough study completion, an average of 90 daysNumber of mechanical ventilator-free day
Vasoactive-free daysThrough study completion, an average of 90 daysNumber of vasoactive-free day
Day of HospitalizationThrough study completion, an average of 90 daysLength of hospital stay and ICU stay
Major adverse kidney events (MAKE) at 30 and 90 days90 daysComposite of all-cause mortality, RRT dependence, and persistent kidney dysfunction
Incidence of adverse events7 daysNumber of adverse events, including catheter-related bloodstream infection, polyuria, arrhythmia, hypotensive episodes, electrolyte and acid-base disturbances, occurring within 7 days after randomization

Countries

Thailand

Contacts

CONTACTPrit Kusirisin, MD
jingprit@hotmail.com+66897574028

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Oct 31, 2026