Chronic heart failure
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1)Subjects who have been hospitalized at least once due to heart failure within the previous t 1 year from the presentl admission. (2)Subjects who can regularly visit medical institutions as outpatients after the discharge. (3)Subjects who can visit the hospital a year after the discharge. (4)Subjects aged 20 and over at the time of obtaining informed consent. (5)Subjects who have fully understand the study participation and sign the informed consent form.
Exclusion criteria
Exclusion criteria: (1)Subjects unable to make an independent judgment about participation in the study. (2)Subjects diagnosed with dementia (3)Subjects who have been already registered with this study (4)Subjects currently participating in other clinical trials (5)Subjects in inappropriate condition for the trial judged by investigators
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The length of time between the date of the baseline and the date of death / admission to the hospital from any cause. | — |
Secondary
| Measure | Time frame |
|---|---|
| The length of time between the date of discharge and the date of cardiac events. The length of time between the date of discharge and the start date of the first non-drug therapy for cardiac events or exacerbation of heart failure. Number of hospitalized days for a year from the date of discharge. Number of hospitalizations for a year from the date of discharge. The level of improvement of QOL Clinical composite response The rate of improvement of natriuretic peptide | — |
Countries
Japan
Contacts
Public Health Research Foundation (PHRF) Comprehensive Support Project for Clinical Research of Lifestyle-Related Disease (CSP-LD)