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Epidemiological Multicenter Study for Tailored Treatment in Heart Failure

Epidemiological Multicenter Study for Tailored Treatment in Heart Failure - ELMSTAT-HF

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000039026
Enrollment
7000
Registered
2020-01-14
Start date
2020-01-14
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart failure

Interventions

None listed

Sponsors

Department of Cardiovascular Medicine, Faculty of Medicine and Graduate School of Medicine, Hokkaido University
Lead Sponsor
Iwate Tohoku Medical Megabank Organization, Iwate Medical University Division of Cardiology, Department of Internal Medicine, Iwate Medical University Tohoku Medical Megabank Organization, Tohoku University Department of Diagnostic Imaging, Hokkaido University Graduate School of Medicine Laboratory of Media Dynamics, Graduate School of Information Science and Technology, Hokkaido University
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: HF arm 1. 20 years of age or older 2. Patients who meet the diagnostic criteria for heart failure in the current heart failure guidelines (JCS 2017,ESC 2016) 3. Patients who give written informed consent AF arm 1. 20 years of age or older 2. Left ventricular ejection fraction of 40% or more 3. NYHA functional class 1 4. Patients who give written informed consent Control 1. Participants in the Tohoku Medical Megabank Project 2. 20 years of age or older at the time of informed consent.

Exclusion criteria

Exclusion criteria: HF arm 1. Sepsis 2. Acute coronary syndrome 3. Acute myocarditis 4. Patients who received heart transplantation or can be candidate for heart transplantation (i.e., patients with left ventricular assist device for waiting heart transplantation) 5. Scheduled for open heart surgery within a month 6. Patients who are considered as inappropriate candidate for this study by the principal investigator AF arm 1. Patients with a history of hospitalization for heart failure 2. Acute coronary symdrome 3. Patients who are considered as inappropriate candidate for this study by the principal investigator Control 1. Diagnosed as atrial fibrillation 2. Diagnosed as heart failure

Design outcomes

Primary

MeasureTime frame
All-cause death Re-admission due to worsening heart failure More than 10% additional reduction on Left ventricular ejection fraction

Secondary

MeasureTime frame
Implantation of ventricular assist device Heart transplantation New-onset atrial fibrillation Stroke Systemic embolism Acute myocardial infarction Hospitalization due to major bleeding Ventricular arrhythmia

Countries

Japan

Contacts

Public ContactToshiyuki Nagai

Faculty of Medicine and Graduate School of Medicine, Hokkaido University Department of Cardiovascular Medicine

nagai@med.hokudai.ac.jp011-706-6973

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026