RecruitingPhase 4NCT04707261
Association Between Dapagliflozin-induced Improvement and Anemia in Heart Failure Patients (ADIDAS)
A Prospective, Randomized, Double-blind, Multicenter Study on the Association Between Dapagliflozin-induced Improvement and Anemia in Heart Failure Patients (ADIDAS)
Sponsor
Xiangtan Central Hospital
Enrollment
1,990 participants
Start Date
Aug 6, 2021
Study Type
INTERVENTIONAL
Conditions
Summary
The primary objective of this study is to investigate the hemoglobin change and association between hemoglobin change and readmissions due to heart failure, and all-cause death in patients with heart failure treated with dapagliflozin or placebo.
Eligibility
Min Age: 18 YearsMax Age: 100 Years
Inclusion Criteria3
- Male or female between the ages of 18 and 100 years.
- Elevated NT-proBNP or BNP levels on admission.
- Ejection fraction of 50% or less, and New York Heart Association (NYHA) class II, III, or IV symptoms.
Exclusion Criteria3
- Treatment with SGLT2-i during the past 3 months of admission,or previous intolerance of an SGLT2 inhibitor.
- Severe (eGFR \<30 mL/min/1.73 m\^2 by CKD-EPI), unstable or rapidly progressing renal disease at the time of randomization.
- Pregnant or breast feeding female patients.
Interventions
DRUGDapagliflozin
Participants will receive dapagliflozin 10 mg once daily
DRUGPlacebo
Participants will receive placebo 10 mg once daily
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT04707261
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