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Efficacy of Benidipine, a Long-acting Dihydropyridine Calcium Channel Blocker, for Dilated Cardiomyopathy Patients with Coronary Vasospasm

Efficacy of Benidipine, a Long-acting Dihydropyridine Calcium Channel Blocker, for Dilated Cardiomyopathy Patients with Coronary Vasospasm - Efficacy of Benidipine for DCM Patients with Coronary Vasospasm

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000021961
Enrollment
60
Registered
2016-04-20
Start date
2015-12-01
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

dilated cardiomyopathy

Interventions

Benidipine, twice a day, 2mg to 8mg per day, for 6 months no intervention

Sponsors

Tohoku University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who are diagnosed as dilated cardiomyopathy definitely or suspiciously and meet following criteria; 1) Ejection Fraction <=40% and >=20%, 2) without valvular disease and significant stenosis or obstruction in coronary arteries, and who are excluded secondary cardiomyopathy by myocardial biopsy, 3) who are in stable status with symptoms of NYHA 1 to 3 within 3 months before intervention

Exclusion criteria

Exclusion criteria: 1) Patients who have ischemic heart disease, valvular disease, acute myocarditis, and secondary cardiomyopathy 2) Patients who have been taking calcium channel blocker 3) Patients in unstable status with symptoms of NYHA 4 4) Patients having serious liver dysfunction or having serious renal dysfunction requiring hemodialysis 5) Patients who are intolerant to dihydropyridine calcium channel blocker 6) Patients with a contraindication to dihydropyridine calcium channel blocker 7) Patients who are pregnant 8) Patients who did not consent to the trial 9) Patients who were considered as inappropriate candidates for the trial by phsicians

Design outcomes

Primary

MeasureTime frame
Ejection Fraction at 6 months after the initiation of the treatment

Countries

Japan

Contacts

Public ContactKatsuya Kozu

Tohoku University Graduate School of Medicine Cardiovascular Medicine

kozu.k@cardio.med.tohoku.ac.jp022-717-7153

Outcome results

None listed

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