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NCT07731490Recruiting

Early Detection and IntervenTion in Heart Failure

Source: ClinicalTrials.gov · Last updated 28 Jul 2026

Brief summary (registry, in English)

Heart failure (HF) occurs when the heart is no longer able to pump blood effectively throughout the body. This leads to symptoms that gradually worsen over time and are often mistaken for normal signs of aging. Because of its insidious onset, early detection is challenging. Both patients and healthcare professionals are often insufficiently aware of the early signs and symptoms of HF, resulting in delayed diagnosis. Consequently, timely initiation of treatments that could slow disease progression, improve quality of life, and reduce hospitalizations is often missed. Although a simple blood test measuring NT-proBNP levels can facilitate the early diagnosis of HF, it is not routinely used in clinical practice. The aim of this study is to evaluate whether a combined strategy for the early diagnosis and treatment of HF can reduce hospitalizations. This strategy includes: 1. increasing awareness of HF among patients and physicians, 2. using NT-proBNP testing for the early detection of HF in high-risk patients, and 3. promptly initiating guideline-directed HF treatment when the diagnosis is confirmed. The researchers will assess whether this strategy effectively reduces hospitalizations due to acute heart failure over an 18-month follow-up period.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
18000 (estimated)
First submitted
9 Jul 2026
Start date
3 Dec 2025
Primary completion date
Apr 2028
Lead sponsor
University Hospital, Basel, Switzerland
NCT number
NCT07731490

What you commit to

  • Study type: Interventional
  • Planned participants: 18000
  • From 3 Dec 2025 to the primary completion date, Apr 2028
  • 21 sites in 9 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previously enrolled in this study.
  • Patients died prior to postinterventional day 1 (8:00 a.m.)

Other illness

  • Dementia documented in the medical history.
  • Metastatic cancer in the medical history.
  • Known allergies, hypersensitivity, or intolerance to SGLT2 Inhibitors / Loop Diuretics / MRA or is excipients.
  • Patients requiring intensive care unit (ICU) or intermediate care (IMC) stay beyond 11:00 a.m. on the first postoperative day or any post-interventional stroke unit stay until 8:00 a.m. on the first postoperative day.

Lab values

  • Estimated glomerular filtration rate (GFR) \<30 mL/min/1.73 m2.

Other

  • Systolic blood pressure ≤ 95 mmHg
  • Known HF.
  • Non-resident in the country of the recruiting site
  • Incapacity of the patient to make judgements
  • Patients not hospitalized overnight
  • Severe aortic or mitral stenosis

Who the study is looking for

  • General consent (GC) has not been rejected.
  • Age ≥ 65 years.
  • Elective percutaneous coronary intervention\* (PCI), pulmonary vein isolation\* (PVI), pacemaker implantation\* (PM, no cardiac resynchronisation), transcatheter aortic valve intervention\* (TAVI), major non-cardiac surgery\* or presenting with tachyarrhythmia to the emergency department (ED) (without a diagnosis of HF within 24h).
    • Exclusion criteria are assessed on day 1 after the procedure

Age in the registry: 65 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (21)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Universitätsklinik für Innere Medizin II
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ViennaAustriaNot yet recruiting
Queen Giovanna University Hospital
Coordinator of this site? Confirm its status
SofiaBulgariaNot yet recruiting
KSA Kantonsspital Aarau
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AarauSwitzerlandNot yet recruiting
Cantonal Hospital Baden
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BadenSwitzerlandNot yet recruiting
St. Claraspital AG
Coordinator of this site? Confirm its status
BaselSwitzerlandNot yet recruiting
University Hospital Basel
Coordinator of this site? Confirm its status
BaselSwitzerlandRecruiting
University Hospital Genève
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GenevaSwitzerlandNot yet recruiting
University Hospital Lausanne
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LausanneSwitzerlandNot yet recruiting
Kantonsspital Luzern
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LucerneSwitzerlandNot yet recruiting
Hospital Istituto Cardiocentro Ticino
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LuganoSwitzerlandNot yet recruiting
Kantonsspital St. Gallen
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Sankt GallenSwitzerlandNot yet recruiting
University Hospital Zurich
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ZurichSwitzerlandNot yet recruiting
Stadtspital Zürich
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ZurichSwitzerlandNot yet recruiting
University Hospital Freiburg-Bad Krozingen
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Freiburg im BreisgauGermanyNot yet recruiting
Universitätsklinikum der Ruhr-Universität Bochum
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HerneGermanyNot yet recruiting
Herzzentrum Leipzig, Klinik für Innere Medizin/Kardiologie
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LeipzigGermanyNot yet recruiting
University Hospital Ramón y Cajal Madrid
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MadridSpainNot yet recruiting
Royal Infirmary Edinburgh
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EdinburghUnited KingdomNot yet recruiting
University Hospital Pisa
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PisaItalyNot yet recruiting
Konkuk University Medical Center
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SeoulSouth KoreaRecruiting
Erasmus MC Rotterdam
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RotterdamNetherlandsNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.