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

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age20+
SponsorChiang Mai University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult 20 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)

Disqualifiers

Use any inotropic drug (norepinephrine, epinephrine, dopamine, dobutamine)

Blood urea nitrogen (BUN) >80 mg/dL

Serum K <3.5 or >5 mmol/L

Arterial potential of Hydrogen (pH) <7.3

Trial design

Design model

Parallel

Treatments tested in this trial

  • Furosemide Injection

    Drug

    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).

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Protocol based-furosemide stress testExperimental treatment 1 intervention
Group B: Standard careNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

% of patients with Renal recovery

Free of RRT for at least 5 days

Time frame
5 days

Secondary outcomes

1

% of patients with Mortality

28 days all cause mortality and in-hospital mortality

Time frame
28 days
2

RRT free days

No need to restart RRT

Time frame
28 days
3

Day of Hospitalization

Length of hospital stay and ICU stay

Time frame
28 days
4

Ventilator-free day

Number of mechanical ventilator-free day

Time frame
28 days

Other outcomes

Sponsors and contacts

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