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Evaluating Adherence to Guideline-Directed Medical Therapy in Patients With Advanced Heart Failure

Key facts

Where
Bergamo és Milan, OlaszországSee the 2 sites

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 75 years old?

Forrás: NCT07560982: ki vehet részt

Where in Olaszország

  • ASST Ospedale Papa Giovanni XXIIIBergamo, OlaszországToborzás még nem indult
  • IRCCS Ospedale San RaffaeleMilan, OlaszországTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Università Vita-Salute San Raffaele
Trial code
NCT07560982
Record updated
2026. július 6.
Original description
A Prospective Observational, Multi-Center, Real-World Pharmacological Study Evaluating Adherence to Guideline-Directed Medical Therapy Using the Four-Pillar Strategy in Patients with Advanced Heart FailureRead full original descriptionShow less

Evaluating Adherence to Guideline- Directed Medical Therapy Using the Four-Pillar Strategy in Patients With Advanced Heart Failure: the Advanced Heart Failure Unified Board (Ad-HUB) Study

A Prospective Observational, Multi-Center, Real-World Pharmacological Study Evaluating Adherence to Guideline-Directed Medical Therapy Using the Four-Pillar Strategy in Patients with Advanced Heart Failure

Inclusion: Age > 18 and < 75 years; Heart failure with left ventricular ejection fraction ≤ 35%; Persistent symptoms of heart failure, New York Heart Association class III or IV; Requirement for high-dose diuretic therapy, specifically Furosemide > 50 mg/day orally as per routine clinical practice; At least one of the following additional indicators of severity or refractoriness:; need for progressive escalation of diuretics,; intolerance to optimized medical therapy,; persistence of symptoms despite advanced treatments such as (but not limited to) cardiac resynchronization therapy (CRT-D)and/or MitraClip; Ability and willingness to provide written informed consent for participation and for the processing of clinical data for research purposes.

Exclusion: Good response to optimized conventional guideline-directed medical therapy; Mild or absent symptoms (New York Heart Association class I-II); Extreme frailty or severe non-reversible disability, or psychiatric or cognitive disorders preventing adherence to follow-up; Left ventricular ejection fraction > 35%; Age ≤ 18 years or ≥ 75 years; Pregnant or breastfeeding women.

ClinicalTrials.gov NCT07560982