Study identifier:D1699R00046
ClinicalTrials.gov identifier:NCT05635331
EudraCT identifier:N/A
CTIS identifier:N/A
Early treatment of heart failure: a non-interventional observational study program of patients with heart failure and initiated on dapagliflozin (EVOLUTION-HF - GREECE)
heart failure
N/A
No
-
All
257
Observational
18 Years - n/a
Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Feb 2025 by AstraZeneca
AstraZeneca
-
Heart failure (HF) is a global, public health issue that affects more than 63 million people worldwide. Despite advancements in treatment, a HF diagnosis still leads to significant morbidity and mortality. Dapagliflozin has been approved by both the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA), in May 2020 and November 2020 respectively, for HF with reduced ejection fraction (HFrEF). The overall aim of this study is to describe the characteristics of patients initiating dapagliflozin for the treatment of HFrEF and to provide early insights into real-world dapagliflozin treatment patterns as well as patient-reported outcomes (PROs) including quality of life.
Location
Location
Athens, Greece, 11527
Location
Thessaloniki, Greece, 54642
Location
Thessaloniki, Greece, 54636
Location
Athens, Greece, 12462
Location
Ioannina, Greece, 45445
Location
Athens, Greece, 14233
Location
Heraclion, Greece, 71409
Location
Chania, Greece, 73300
Arms | Assigned Interventions |
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