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Best Beta-Blocker in Systolic Heart Failure, analysis of prognosis and evaluation of therapies

Best Beta-Blocker in Systolic Heart Failure, analysis of prognosis and evaluation of therapies - B-cube SHF trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000023944
Enrollment
400
Registered
2016-09-07
Start date
2016-06-01
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

systolic heart failure

Interventions

Bisoprolol group Daily oral administration of bisoprolol 0.625 mg tablet once a day should be given. If tolerability is confirmed by an investigator, the dose should be increased to 1.25 mg. In t

Sponsors

Chiba-Nishi General Hospital Cardiology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) primary disease: in principle, ischemic heart disease or dilated cardiomyopathy. 2) heart failure patients with 40% or less of left ventricular ejection fraction (LVEF). any NYHA class. 3) basic treatment: in principle, patients undergoing treatment with an ACE inhibitor(or ARB) OR a diuretic. 4) patients who had not undergone treatment with a beta-blocker (except eye drops) within 8 weeks before the registration date. 5) age: patient aged 20 to less than 85 on the day of obtaining written informed consent. 6) hospitalized/outpatient: either hospitalized or outpatient status. 7) gender: male of female 8) patients who had a detailed briefing of the trial with explanatory documents prior to the enrollment and voluntarily signed a consent form.

Exclusion criteria

Exclusion criteria: 1) patients who are considered not to be candidate for administration of beta blocker. 2) patients who are scheduled to undergo emergent dialysis or chronic dialysis patients. 3) patients who have developed acute coronary syndrome within 8 weeks before the registration day. 4) patients who need mechanical hemodynamical support (except for pace maker implantation OR ICD) 5) patients who have malignancy within 1 year prognosis. 6) patients who are pregnant, lactating, may become pregnant, or want to become pregnant during the study. 7) patients who are judged by an investor to be inappropriate for this study for any other reason.

Design outcomes

Primary

MeasureTime frame
The composite endpoint of major adverse cardiac events (MACEs) OR rehospitalization for heart failure

Secondary

MeasureTime frame
safety

Countries

Japan

Contacts

Public ContactHiroyuki Yamamoto

Chiba-Nishi General Hospital Cardiology

hyamamoto@chibanishi-hp.or.jp047-384-8229

Outcome results

None listed

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