Acetazolamide or Metolazone in Acute Heart Failure

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorClinica Alemana de Santiago

About this trial

Impact of Acute Heart Failure:

According to the World Health Organization (WHO), approximately 26 million people suffer from Heart Failure (HF), with a mortality rate of up to 50% within five years of diagnosis. Acute Heart Failure (AHF) exacerbations, leading to hospitalization, are common and represent the primary cause of hospital admissions in those over 65. Effective decongestion during hospitalization is crucial, as failure to achieve it doubles the risk of rehospitalization and mortality, incurring significant healthcare costs.

Use of Diuretics in Acute Heart Failure:

Diuretics, particularly loop diuretics like furosemide, are a cornerstone in managing AHF by inducing natriuresis and achieving decongestion. Clinical experience supports their use, though limited clinical trials exist. Pharmacological concepts guide their administration, emphasizing intravenous delivery in high doses and adjusting subsequent doses based on decongestive efficacy. Additionally, sequential tubular blockade with other diuretics like metolazone and acetazolamide is explored to enhance decongestion.

Use of Metolazone and Acetazolamide:

Sequential tubular blockade, using metolazone and acetazolamide in conjunction with furosemide, aims to achieve rapid and effective decongestion. While metolazone targets the distal tubule, inhibiting sodium-chloride channels, acetazolamide affects proximal tubular function. Studies like ADVOR (acetazolamide) and CLOROTIC (thiazide-like diuretic) demonstrate the potential benefits of combining these diuretics for quicker decongestion but with potential risks (in the case of Hydrochlorothiazide).

Outcomes Measured by Major Studies:

Recent studies assessing decongestion in AHF reveal a lack of uniformity in outcome selection. The primary focus should be on reducing rehospitalizations and post-discharge mortality by achieving effective decongestion. The ADVOR study, using a simple congestion score based on clinical and imaging criteria, underscores the importance of reaching a congestion score of 0 or 1 promptly.

Congestion Monitoring:

Monitoring diuretic treatment solely based on clinical aspects may not capture subclinical congestion, necessitating biochemical and imaging parameters. The ACME-AHF trial proposes a diagnostic score integrating clinical and imaging aspects to evaluate congestion status. Secondary outcomes include cumulative diuresis, weight loss, diuretic efficiency, and natriuresis, with a focus on natriuresis as a reliable physiological parameter for decongestion.

Aim of the study:

The ACME-AHF trial is designed to compare the efficacy and safety of two diuretic combination strategies: acetazolamide with furosemide and metolazone with furosemide. The primary objective is to relieve congestion, assessed using a congestion score, within the first three days of treatment during an hospitalization for acute heart failure.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Acute heart failure: Hospitalization due to symptoms of heart failure, congestion signs documented with a congestion score greater than 1, NT-proBNP above 1000 pg/ml.

Randomization within 24 hours of admission.

Disqualifiers

Under 18 years of age.

Received more than one dose of intravenous furosemide before randomization.

Cause of heart failure: hypertrophic or restrictive cardiomyopathy, or constrictive pericarditis.

Acute coronary syndrome or severe acute valvulopathy as the cause of decompensation.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Acetazolamide 250 MG

    Drug

    Acetazolamide 250mg orally per day plus furosemide as per protocol. The intervention is administered on the day of hospital admission and for two consecutive mornings. The total intervention consists of 3 doses. The intervention is discontinued on the third morning. The calculation of the congestion score is performed every morning until the third morning. If complete decongestion is achieved, the primary outcome will be considered fulfilled.

  • Metolazone 2.5 MG

    Drug

    Metolazone 2.5mg orally per day plus furosemide as per protocol. The intervention is administered on the day of hospital admission and for two consecutive mornings. The total intervention consists of 3 doses. The intervention is discontinued on the third morning. The calculation of the congestion score is performed every morning until the third morning. If complete decongestion is achieved, the primary outcome will be considered fulfilled.

  • Furosemide Injection

    Drug

    Intravenous furosemide in a double daily dose. The dosage is determined by a predefined table based on the admission renal function and the outpatient dose prior to admission. In general terms, for patients with an estimated glomerular filtration rate above 60 ml/min/1.73m² or those experiencing heart failure debut, the dose will be 1x the outpatient dose. For those with a glomerular filtration rate below 60 ml/min/1.73m², the dose will be 2x the outpatient dose. The dosing protocol for this arm also serves as guidance for furosemide in the intervention arms.

Treatment groups

1,050 Participants
are divided into 3 treatment groups
Group A: Furosemide aloneActive comparator 1 intervention
Group B: Acetazolamide plus FurosemideExperimental treatment 2 interventions
Group C: Metolazone plus FurosemideExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Treatment success

Complete decongestion by the third morning without requiring escalation in diuretic therapy (by the second morning).

Time frame
4 days

Secondary outcomes

1

Mortality

All-cause mortality during the first 3 months after start of the study

Time frame
3 months
2

Worsening Heart Failure

Readmission for Heart Failure or Urgent visit for Heart Failure during the first 3 months after start of the study

Time frame
3 months
3

Cumulative 24-hour Natriuresis

Natriuresis measured on the second day

Time frame
Day 2
4

Cumulative weight loss

Cumulative weight loss by the third morning

Time frame
4 days

Other outcomes

1

Any adverse event

Any adverse clinical event related to intervention during the first 3 months after start of the study

Time frame
3 months
2

Changes in pH value

Change in pH over the specified time period

Time frame
4 days
3

Change in plasma electrolyte values

Change in plasma concentration of sodium, potassium, and chloride

Time frame
4 days

Locations

This trial has no locations.

Sponsors and contacts

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