Study identifier:D1699R00030
ClinicalTrials.gov identifier:NCT05250011
EudraCT identifier:N/A
CTIS identifier:N/A
Early Treatment of Heart Failure: a Non-Interventional Observational Study of Italian Patients with Heart Failure and Initiated on Dapagliflozin
Heart Failure, Reduced Ejection Fraction
N/A
No
Dapagliflozin
All
252
Observational
18 Years - n/a
Allocation: Non-randomized
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Mar 2025 by AstraZeneca
AstraZeneca
Fullcro s.r.l.
This is an observational, non-interventional, longitudinal prospective descriptive study including participants diagnosed with Heart Failure with reduced Ejection Fraction (HFrEF) in Italy and initiated on treatment with dapagliflozin according to the approved HFrEF indication. The study is aimed at providing insights into real-world drug utilization and treatment patterns of dapagliflozin in the Italian HFrEF setting, as well as patient-reported outcomes including quality of life.
Heart failure (HF) is a significant burden for public health, affecting more than 63 million people worldwide and expected to increase as the population ages; in Italy, the estimated prevalence of HF is 1-3% and the incidence rate 2-5 cases per 1000 persons per year. Despite advancements in treatment, a HF diagnosis still leads to significant morbidity and mortality and impacts on patients’ quality of life (QoL). Dapagliflozin is the first in a novel class of glucose-lowering agents known as sodium-glucose co-transporter-2 (SGLT2) inhibitors, approved for the treatment of Heart Failure with reduced Ejection Fraction (HFrEF). As with all new drugs introduced into clinical practice, there is a strong scientific interest in producing evidence from observational studies regarding the use of dapagliflozin for the treatment of HFrEF in real-world settings with detailed clinical data on heart failure symptoms, outcomes, and health-related QoL. The overall aim of this observational study is to describe the characteristics of patients in Italy initiating dapagliflozin for the treatment of HFrEF and to provide early insights into real-world dapagliflozin treatment patterns (primary objectives) as well as patient-reported outcomes including quality of life (secondary objectives). This study is part of a multicountry study programme, including similar studies that will be conducted in other countries with similar objectives. Data from each of the individual studies may be combined in a pooled analysis.
Location
Location
Brescia, BS, Italy, 25123
Location
Roma, RM, Italy, 00163
Location
Napoli, na, Italy, 80131
Location
Foggia, FG, Italy, 71122
Location
Genova, GE, Italy, 16132
Location
Firenze, FI, Italy, 50100
Location
Catanzaro, CZ, Italy, 88100
Location
Roma, RM, Italy, 00189
Arms | Assigned Interventions |
---|---|
Single-cohort Patients initiated on dapagliflozin according to the approved indication for heart failure with reduced ejection fraction (HFrEF) and current medical practice | - |
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