Patients with heart failure who finished the PARALLEL-HF trial
Conditions
Interventions
None listed
Sponsors
Department of Cardiology, Iwate Prefectural Central Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: patients with chronic HF in our hospital participated in the PARALLEL-HF trial
Exclusion criteria
Exclusion criteria: Patients who did not consent to participate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint was percent change (%Change) from baseline to week 24 in plasma A-, B-, and N-terminal pro-B-type natriuretic peptide (ANP, BNP, and NT-proBNP) levels. | — |
Secondary
| Measure | Time frame |
|---|---|
| The second endpoint was the change in echocardiographic parameters related to myocardial remodeling from the baseline to week 24. | — |
Countries
Japan
Contacts
Public ContactAkihiro Nakamura
Iwate Prefectural Central Hospital Department of Cardiology
Outcome results
None listed