acute heart failure
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Hospitalized acute heart failure patients with volume overload Subjects with NYHA functional classification II-IV Subjects with Furosemide > 40mg/day Serum sodium level < 140mEq/L Agreement with written informed consent
Exclusion criteria
Exclusion criteria: Subjects with hemodialysis or anuria Subjects with acute coronary syndrome, pregnancy, malignancy, or previously administration of Tolvaptan
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| change of congestion scale (7 consecutive days from administration) | — |
Secondary
| Measure | Time frame |
|---|---|
| serial change of renal function (7 consecutive days after administration) urine volume (7 consecutive days after administration) weight change (7 consecutive days after administration) serial change of other laboratory markers(7 consecutive days after administration) prognosis(30-day, 6-month) | — |
Countries
Japan
Contacts
Kasugai Municipal Hospital Department of Cardiology