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2024-513448-26-00CompletedPhase 4

Effects of Digoxin in Modern Heart Failure Treatment

Source: EU CTIS (euclinicaltrials.eu) · Last updated 7 Apr 2026

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Brief summary (registry, in English)

To assess the effectiveness of Digoxin in functional capacity and cardiac function when combined with standard of care modern heart failure treatment.

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
50 (actual)
First submitted
8 Jul 2024
Start date
29 Oct 2024
Lead sponsor
Unidade Local De Saude De Sao Jose E.P.E.
EU CT number
2024-513448-26-00

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 50
  • 1 site 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

  • Already using Digoxin or having used it on the last 9 days (washout period).
  • New heart failure medication in the previous 6 months.
  • Change in class I HF dose (ARNi, ACEi, ARB, beta-blockers, SGLT2 inhibitors or MRA) in the previous 3 months.

Other illness

  • Arrhythmias caused by cardiac glycoside intoxication
  • Sick sinus syndrome without pacemaker or Implantable cardioverter-defibrillators (ICD).
  • Wolff-Parkinson-White syndrome.
  • Heart rate below 55 bpm at rest in sinus rhythm or below 70 bpm in AF in patients without CRT or cardiac physiologic pacing.
  • Hypersensitivity to Digoxin, other digitalis glycosides or to any of the excipients

Lab values

  • Recent (<6 months): myocardial infarction, coronary revascularization, surgery or catheter intervention for valvular heart disease, stroke, or cerebral ischaemia, start of heart failure device therapy potentially improving left ventricular ejection fraction or HF symptoms (e.g. cardiac resynchronization therapy, cardiac contractility modulation, baroreflex activation therapy)
  • Significant renal insufficiency (Glomerular filtration rate (GFR) ≤ 15mL/min) as evaluated by the Cockcroft-Gault formula.
  • Persistent potassium below 3.2 mmol/L.

Age

  • Age < 18 years old.

Other

  • Pregnant or lactating women. Woman of childbearing potential who do not accept to use the methods of contraception suggested for the trial.
  • NTproBNP values < 125pg/mL.
  • Ventricular tachycardia or ventricular fibrillation
  • Persistent hypercalcaemia or hypomagnesaemia.
  • Grade II-III AV block without a pacemaker or ICD.

Who the study is looking for

  • Chronic heart failure with reduced ejection fraction (LVEF ≤45%) with at least 6 months of maximally tolerated class I medications (ARNi or ACEiplus beta-blockers plus SGLT2 inhibitors plus MRA) unless contraindicated.
  • Symptomatic heart failure with at least New York Heart Association (NYHA) class ≥ II in which Digoxin may be considered according tocurrent European Guidelines.
  • Age ≥ 18 years old.
  • Ability to provide informed consent and willingness to comply with studyprocedures.

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

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (1)

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

SiteCityCountrySite status
Unidade Local De Saude De Sao Jose E.P.E.LisbonPortugalCompleted

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