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Furosemide Stress Test for the Prediction of Acute Kidney Injury Severity in Acute Heart Failure Patients

Furosemide Stress Test for the Prediction of Acute Kidney Injury Severity in Acute Heart Failure Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04464811
Enrollment
257
Registered
2020-07-09
Start date
2020-07-05
Completion date
2021-08-31
Last updated
2020-07-09

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

Conditions

Acute Kidney Injury, Heart Failure

Brief summary

This study is aim to study the changes of serum creatinine levels at 72 hours after admission in patients with acute heart failure who has diuretic resistance compared to those who do not have diuretic resistance from furosemide stress test

Detailed description

This study is an observational prospective study to demonstrate a prognosis of acute heart failure patients who have diuretic resistance compared to those who do not have diuretic resistance from furosemide stress test. The primary outcome is changes of serum creatinine levels at 72 hours compared to baseline values at the time of admission.

Interventions

DIAGNOSTIC_TESTFurosemide stress test

Furosemide stress test is performed by administration of intravenous furosemide 1 mg/kg in patients who do not receive oral furosemide before and 1.5 mg/kg patients who have never received oral furosemide.

Sponsors

Chiang Mai University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Age ≥18 years * Diagnosis of acute heart failure which is defined by 2 of the 3 following features: ≥2+ leg edema, jugular venous pressure \>10 cm from physical examination or central venous pressure \>10 mmHg, and bilateral pulmonary edema or bilateral pleural effusion from chest radiography * Patients consent to participate into the study

Exclusion criteria

* Patients who receive furosemide ≥500 mg/day or hydrochlorothiazide ≥100 mg/day or spironolactone ≥100 mg/day or tolvaptan of any doses * Patients who have systolic blood pressure \<100 mmHg or who need vasoactive drugs inotropic agents (except dobutamine) * Patients with intravascular volume depletion from clinical evaluation * Patients with chronic kidney disease stage 5 (estimated glomerular filtration rate \<15 ml/min/1.73 m2) or patients who receive maintenance dialysis * Patients who require renal replacement therapy at the time of admission * Patients whom diagnosed hypertrophic obstructive cardiomyopathy, severe valvular stenosis or complex congenital heart disease * Patients with sepsis or systemic infection * Pregnant women * Patients who have history of furosemide, spironolactone or hydrochlorothiazide allergy

Design outcomes

Primary

MeasureTime frameDescription
Serum creatinineSeventy-two hours after admissionChanges in serum creatinine from baseline

Secondary

MeasureTime frameDescription
Requirement for renal replacement therapyDuring hospital admission periodRenal replacement therapy is defined as any mode of dialysis or extracorporeal therapy to treat volume overload for heart failure
Length of hospital admissionDuring hospital admission periodNumbers of days that patients need to stay in the hospital
Serum creatinineDay 7 of hospital admissionChanges in serum creatinine from baseline
Numbers of hospital readmissionMonth 1 and 3 after hospital dischargeReadmission to the hospital due to heart failure
Mortality rateDay 7 and 28 after hospital admissionConfirmed death
Changes of the stage of heart failure defined by New York Heart Association (NYHA) classificationDay 7 and 28 after hospital admissionHeart failure stage defined by New York Heart Association (NYHA) classification

Countries

Thailand

Contacts

Primary ContactKajohnsak Noppakun, MD
kajohnsak.noppakun@cmu.ac.th+66815953465
Backup ContactTiranun Suriya, RN
tingsuri@hotmail.co.th+66818812106

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026