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Testing a urine sodium guided diuretic plan in acute heart failure

Tests a urine sodium guided water pill plan in adults hospitalized with acute heart failure.

Plain-language title generated from the registry record
Registry title: Investigating a Tailored Diuretic Algorithm in Acute Heart Failure Patients

Key facts

Where
Breda and Heerlen, NetherlandsSee the 2 sites

Where in Netherlands

  • Amphia ZiekenhuisBreda, NetherlandsTaking people
  • Zuyderland MCHeerlen, NetherlandsTaking people

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Trial details

Who runs it
Zuyderland Medisch Centrum
Trial code
NCT06092437
Record updated
13 April 2026
Original description
Acutely decompensated heart failure (ADHF) is highly prevalent and has a high (financial) burden on the health care system. Treatment often consists of the administration of IV decongestive agents. Adequate dosing is difficult due to varying diuretic resistance and inadequate parameters to evaluate the response. Urine sodium is a promising biomarker to evaluate the diuretic response. It is hypothesized that a tailored, urine sodium guided diuretic algorithm will result in faster and more complete decongestion and therefore lead to better survival (in terms of mortality and heart failure events) while being non-inferior in terms of safety (mainly regression of kidney function).Read full original descriptionShow less

TAILOR-AHF: Randomized Trial Investigating a Tailored Diuretic Algorithm in Acute Heart Failure Patients

Acutely decompensated heart failure (ADHF) is highly prevalent and has a high (financial) burden on the health care system. Treatment often consists of the administration of IV decongestive agents. Adequate dosing is difficult due to varying diuretic resistance and inadequate parameters to evaluate the response. Urine sodium is a promising biomarker to evaluate the diuretic response. It is hypothesized that a tailored, urine sodium guided diuretic algorithm will result in faster and more complete decongestion and therefore lead to better survival (in terms of mortality and heart failure events) while being non-inferior in terms of safety (mainly regression of kidney function).

Inclusion: Age > 18 years; HF (HFrEF, HFmrEF or HFpEF) diagnosed according to the 2021 HF Guidelines of the European Society of Cardiology [5]; Presentation with AHF meaning at least one symptom (dyspnea, orthopnea, or edema) and one sign (rales, peripheral edema, ascites, or pulmonary vascular congestion on chest radiography) of AHF; An elevated NT-proBNP >300pg/ml; Requiring the need for iv diuretics.

Exclusion: Patients included in other investigational studies regarding heart failure; Presentation with cardiogenic shock or respiratory insufficiency or another reason requiring admission to the intensive care unit upon admission (IC transfer later in the hospitalization is not an exclusion); Terminal renal insufficiency defined as: dialysis patients or eGFR (estimated glomerular filtration rate) < 10 mL/min/1.73 m2.

ClinicalTrials.gov NCT06092437