Skip to content

Beta-Blocker Withdrawal in Heart Failure with Preserved Ejection Fraction and Chronotropic Incompetence (BRILLIANT)

Beta-Blocker Withdrawal in Heart Failure with Preserved Ejection Fraction and Chronotropic Incompetence (BRILLIANT): A Multicenter, Prospective, Randomized, Open-Label, Blinded Endpoint (PROBE) Trial - BRILLIANT trial

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1031210030
Enrollment
150
Registered
2021-04-09
Start date
2021-07-07
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 with preserved ejection fraction

Interventions

Beta-blocker withdrawal or dose reduction

Sponsors

Obokata Masaru
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Age equal to or more than 20 years old 2) Patients with established HFpEF or subjects who are suspected of HFpEF 3) Subjects who are treated with a pre-specified minimum dose of beta-blockers 5) Subjects who are able to keep cycle ergometry exercise (0 watts) for more than 30 seconds 6) Patients who give written consent to participate in this study

Exclusion criteria

Exclusion criteria: 1) Patients with mimic HFpEF: More than mild aortic or mitral valve stenosis, more than moderate aortic or mitral valve regurgitation, history of left ventricular ejection fraction less than 40%, non-group II pulmonary hypertension, hypertrophic cardiomyopathy (except for apical hypertrophic cardiomyopathy), cardiac sarcoidosis, constrictive pericardititis 2) Patients with comorbidities contraindicated for exercise testing: acute decompensated heart failure, acute coronary syndrome, severe coronary artery disease 3) Patients who are expected to have disadvantages in discontinuing beta-blockers: History of old myocardial infarction, presence of obvious myocardial ischemia, appearance of new wall motion abnormality during exercise, history of hospitalization due to tachyarrhythmia within 6 months, Basedow's disease 4) Patients who cannot exercise their legs due to abnormalities in joints, muscles, etc. 4) Patients who are judged to be unsuitable for th e study by the investigators

Design outcomes

Primary

MeasureTime frame
Change in peak oxygen consumption during exercise stress echocardiography from baseline to four-weeks after the intervention

Secondary

MeasureTime frame
*Changes in the following parameters from baseline to four-weeks after the intervention will be assessed: Heart rate during peak exercise Cardiac output during peak exercise Mitral s' during peak exercise GLS during peak exercise VE/VCO2 slope NT-proBNP levels *The following prognostic data will be also assessed: Time to first heart failure hospitalization Time to all-cause mortality Time to cardiac death Time to first heart failure hospitalization or all-cause mortality Time to first heart failure hospitalization or cardiac death

Contacts

Public ContactMasaru Obokata

Gunma University Hospital

obokata.masaru@gunma-u.ac.jp+81-272208145

Outcome results

None listed

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