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Urinary sodium to manage patients with acute heart failure

Evaluating the role of urinary sodium in the management of acute heart failure

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12621000950864
Enrollment
60
Registered
2021-07-21
Start date
2021-10-01
Completion date
2022-08-31
Last updated
2023-02-20

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

Conditions

None listed

Brief summary

Heart failure is one of the most common causes of hospital admissions globally. Typical signs and symptoms of acute heart failure (HF) are mostly related to congestion, driven by sodium retention and subsequent fluid retention. Removal of excess sodium and water (decongestive therapy) by diuretics is the cornerstone of treatment. Assessing the efficacy of treatment by current methods, such as weight loss and net fluid balance is very challenging. Diuretics act by diminishing sodium reabsorption at different sites in the kidney, thereby increasing urinary sodium and water loss. Hence, a limited number of small prospective observational studies have suggested the role of urinary sodium content (UNa) as a tool to rapidly assess the response to decongestive therapy and to estimate future outcomes. Aims and Objectives: 1. To assess the feasibility and efficacy of adjusting diuretic therapy using UNa in patients presenting with AHF in an Australian metropolitan hospital 2. To evaluate the safety of this method 3. To determine if UNa guided diuretic therapy improves clinical outcomes Design: A prospective, randomized controlled trial. Study population 60 patients >18 years old admitted under cardiology team with the primary diagnosis of AHF, requiring intravenous diuretics. Recruitment period: 6month. Expected number: 60 patients.

Interventions

Urinary sodium test will be obtained from acute heart failure patients admitted to the hospital at presentation and within the first 6 hours after the commencement of loop diuretic, then 6-hourly, for the first 48 hours. Diuretics dose will be adjusted by a cardiologist based on urinary sodium and will be given by the ward nurse. Urinary sodium samples will be obtained by ward staff. Interventions will be recorded in patients' medical charts. This adjustment to the timing of taking the first UNa

Urinary sodium test will be obtained from acute heart failure patients admitted to the hospital at presentation and within the first 6 hours after the commencement of loop diuretic, then 6-hourly, for the first 48 hours. Diuretics dose will be adjusted by a cardiologist based on urinary sodium and will be given by the ward nurse. Urinary sodium samples will be obtained by ward staff. Interventions will be recorded in patients' medical charts. This adjustment to the timing of taking the first UNa after the administration of IV diuretic was made after recruiting the first 15 patients.

Sponsors

Metro North Health, TPCH
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

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

Inclusion criteria

at least 18 years old, admitted under cardiology team with the primary diagnosis of acute heart failure

Exclusion criteria

1. Haemodynamically unstable patients, requiring inotropic or mechanical circulatory support 2. Patients with severe kidney dysfunction, on dialysis, or aneuric patients 3. Unable to provide informed consent

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 6, 2026