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OpenTrials
Enrolling by Invitation

NCT Number: NCT07320677

Finding Heart Failure in Those Prescribed Loop Diuretics in Primary Care in Jersey

The goal of this clinical trial is to learn whether a simple blood test screening pathway can help diagnose heart failure earlier in adults in primary care who take loop diuretic medicines (such as furosemide or bumetanide) but do not have a recorded diagnosis of heart failure.

The main questions it aims to answer are:

1. Does offering a NT-proBNP blood test to eligible patients increase the number of new heart failure diagnoses within 12 months compared with usual care? 2. Does this screening pathway also uncover other important heart problems, such as irregular heart rhythms (arrhythmias) or valve disease?

This is a cluster randomised controlled trial, which means that whole GP practices, rather than individual patients, are randomly assigned to one of two approaches:

1. NT-proBNP screening pathway, in which eligible patients are invited for a NT-proBNP blood test 2. Usual care, in which patients continue to be managed as they normally would without proactive screening

Participants will:

Be identified from GP records if they are prescribed loop diuretics and have no prior diagnosis of heart failure

In screening practices, be invited to attend for a free finger-prick NT-proBNP blood test and brief questionnaire

Be referred to the heart failure team and invited for an echocardiogram (a heart ultrasound scan) and further assessment if their NT-proBNP level is higher than 125 pg/mL

Researchers will compare outcomes between screening and usual-care practices after 12 months, focusing on new diagnoses of heart failure. They will also look at other important cardiovascular findings, such as new arrhythmias, valve disease, and heart failure hospitalisation rates.

Enrolling by Invitation

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Jersey General Hospital

Saint Helier, Jersey

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Receiving a loop diuretic (furosemide, bumetanide or torsemide)
  • No coded diagnosis of heart failure in GP records
  • Never had a natriuretic peptide test
  • Willing to have a blood test for NT-proBNP

Exclusion criteria

  • Clinical Frailty Score 7 or above on Rockwood frailty scale
  • Prior diagnosis of heart failure
  • Prior natriuretic peptide testing

Treatment and study plan

NT-proBNP screening

Diagnostic Test

Patients in the intervention arm will be invited for a free point of care NT-proBNP blood test

Primary outcomes

  1. New Heart Failure diagnosis at 12 months

    Time frame: 12 months from practice enrollment

Secondary outcomes

  1. New clinically relevant cardiovascular disease

    Time frame: 12 months

    This will include moderate valvular disease and arrhythmia (eg, AF).

  2. Heart Failure Hospitalisations

    Time frame: 12 months

  3. All cause mortality

    Time frame: 12 months

Other outcomes

  1. Number of patients with heart failure but not coded in primary care record

    Time frame: 12 months

Sponsors and collaborators

Lead sponsor

Government of Jersey

Other Gov

Registry information

Official study title

Finding Heart Failure in Those Prescribed Loop Diuretics in Primary Care in Jersey (FIND-HF LOOP)

Acronym: FIND HF LOOP

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Jan 6, 2026
Registry last updated
Jan 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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