Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07369856

Spot Analysis of Natriuresis to Guide up- or Down-titration of Diuretic Therapy in Ambulatory Patients With Chronic Heart Failure

Led by Cardiology Research UBC · Updated on 2026-03-27

300

Participants Needed

1

Research Sites

112 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Heart failure is a chronic condition that causes congestion and frequent hospitalizations. Diuretic doses are usually adjusted based on clinical judgment without an objective measure of response. This study will test the feasibility of using point-of-care urine sodium measurements to guide up-titration or down-titration of loop diuretics in ambulatory patients with heart failure. Participants will be assigned to one of three groups based on congestion status. Groups 1 and 2 will be randomized 1:1 to natriuresis-guided therapy or standard care. Group 3 will be observational. The 90-day pilot trial will evaluate feasibility, clinical outcomes, and usability of a urine sodium-guided titration strategy.

CONDITIONS

Official Title

Spot Analysis of Natriuresis to Guide up- or Down-titration of Diuretic Therapy in Ambulatory Patients With Chronic Heart Failure

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosis of heart failure according to the Universal Definition
  • Use of loop diuretics
  • Residing in Vancouver Coastal Health (VCH) or Providence Health Care (PHC) regions
  • Group 1: Congestion score 5 or higher OR objective evidence of congestion; stable furosemide use for at least 1 week
  • Group 2: New York Heart Association (NYHA) class I-II; congestion score less than 5; no recent heart failure hospitalization; stable furosemide use for at least 1 month
  • Group 3: First 100 eligible patients not meeting criteria for Groups 1 or 2
Not Eligible

You will not qualify if you...

  • Estimated glomerular filtration rate (eGFR) less than 20 mL/min/1.73m²
  • Receiving renal replacement therapy
  • High-risk clinical status requiring hospitalization
  • Unable to consent or perform required urine sampling

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Vancouver General Hospital

Vancouver, British Columbia, Canada

Actively Recruiting

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Research Team

N

Natalie Bloch, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

5

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