PRospect trial to elucidate the utility of EchocarDIography-based Cardiac ouTput in acute heart failure (PREDICT) study
Not Applicable
- Conditions
- Acute heart failure
- Registration Number
- JPRN-UMIN000039687
- Lead Sponsor
- Hokkaido University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 292
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with acute coronary syndrome, those need for hemodialysis, and those who had been already received positive inotropic agents before the index echocardiography.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Worsening heart failure defined as need for initiation of positive inotropic agents within 7 days after the admission
- Secondary Outcome Measures
Name Time Method Worsening renal function defined as an increase in serum creatinine of 0.3 mg/dL during the treatment, time duration for bed rest, inhospital duration, and all cause mortality during the hospital treatment.