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Efficacy of Ibabradine and Beta-blocker Therapy in Patients with Heart Failure with Reduced Ejection Fraction

Efficacy of Ibabradine and Beta-blocker Therapy in Patients with Heart Failure with Reduced Ejection Fraction - None

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs041200027
Enrollment
40
Registered
2020-07-08
Start date
2020-11-02
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 tachycardia, cardiomyopathy

Interventions

We will randomize the patients with heart failure with reduced left ventricular ejection fraction into the ibabradine arm and the control arm and follow them for six months.
D046650
bradycardia, tachycardia

Sponsors

Kinugawa Koichiro
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Heart failure with reduced left ventricular ejection fraction due to ischemic or non-ischemic cardiomyopathy 2. Refractory to the up-titration of beta-blocker due to failing symptom 3. Sinus rhythm, heart rhythm above 75 bpm, and systolic blood pressure above 90 mmHg 4. New York Heart Association functional class III or IV

Exclusion criteria

Exclusion criteria: 1. Those with a plan of surgical interventions during the observational period 2. Allergy to the beta-blocker 3. Heart rate below 75 bpm or systolic blood pressure below 90 mmHg 4. Chronic obstructive pulmonary disease or bronchial asthma is not a contraindication

Design outcomes

Primary

MeasureTime frame
A daily dose of beta-blocker equivalent to the carvedilol at six months

Secondary

MeasureTime frame
Six-month left ventricular end-diastolic diameter and ejection fraction Six-month plasma B-type natriuretic peptide level Six-month six-minute walk distance Six-month readmission due to heart failure

Contacts

Public ContactKoichiro Kinugawa

Toyama University Hospital

kinugawa@med.u-toyama.ac.jp+81-76-434-7297

Outcome results

None listed

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