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2025-522560-32-01RecruitingPhase 4

A trial investigating partial withdrawal of heart failure therapy in patients with heart failure in remission.

A prospective, randomized, controlled clinical pilot trial investigating the partial down-titration of guideline-directed medical therapy in patients with heart failure in remission

Source: EU CTIS (euclinicaltrials.eu) · Last updated 9 Oct 2026

Next steps

Brief summary (registry, in English)

To investigate the safety and feasibility of heart failure therapy down-titration versus therapy continuation in patients with heart failure in remission.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
100 (estimated)
First submitted
11 Aug 2025
Start date
1 Mar 2026
Lead sponsor
Ziekenhuis Oost Limburg
EU CT number
2025-522560-32-01

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 100
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Recent major cardiovascular events such as an acute coronary syndrome, CABG, stroke or TIA in the 90 days before screening
  • Any sustained ventricular arrythmias within 6 months prior to screening

Other illness

  • Albuminuric chronic kidney disease
  • Uncontrolled hypertension
  • Atrial fibrillation or atrial flutter with a resting heart rate >110 beats per minute
  • Patients with a cardiac resynchronization therapy device who have < 98% biventricular pacing during screening
  • Any untreated valvular heart disease of moderate or greater severity during screening.

Age

  • Presence of any other disease with a life expectancy of < 2 years.

Other

  • Pregnant or lactating women.

Who the study is looking for

  • Adults aged ≥ 18 years
  • Heart failure in remission, defined as heart failure with an improved ejection fraction to an LVEF above 50%, with normalized LV volumes, an NT-proBNP ≤ 250 pg/mL, normal functional capacity, and clinical stability
  • Patients must receive at least 3 HF therapies (ACEi/ARB/ARNI, BB, and MRA or SGLT2i) for HF, consistent with international HF guidelines. Each therapy must have been titrated to the maximally tolerated dose, stable for at least 6 months prior to screening

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (3)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Ziekenhuis Oost-LimburgGenkBelgiumRecruiting
JESSA ZiekenhuisHasseltBelgiumRecruiting
AZ TurnhoutTurnhoutBelgiumRecruiting

Are you the coordinator? Confirm the details

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