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Prospective randomized trial for optimizing medical therapy after coronary stenitng

Prospective randomized trial for optimizing medical therapy after coronary stenitng - Calcium-Beta

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000008321
Enrollment
100
Registered
2012-07-03
Start date
2012-06-01
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

Coronary artery disease (CAD)

Interventions

calcium channel blockers (CCBs) Beta blockers

Sponsors

Keio University, School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients with stable/unstable angina or silent ischemia who underwent PCI with everolimus eluting stent. 2.Single vessel disease with deployment of 3 stents or less. 3.Patients must be 20 years of age or more.

Exclusion criteria

Exclusion criteria: 1.Stent restenosis or previous bypass surgery. 2.Previous diagnosis of vasospasmic angina within 1 years and/or on treatment. 3.Previous PCI within 1 years. 4.An event of acute myocardial infarction within 7 days. 5.Left main disease. 6.Left ventricular ejection fraction of less than 35%. 7.Previous Pacemaker Implant or AV block of more than 1st degree. 8.SBP less than 100 or HR less than 60 prior to PCI. 9.Renal failure (Cr more than 2.0mg/dl or on hemodialysis) 10.Liver failure (eg. cirrhosis) 11.Reversible obstructive lung disease 12.Diagnosis of malignancy within 5 years 13.Pregnancy

Design outcomes

Primary

MeasureTime frame
Presence of Acetylcholine induced coronary vasospasm 9 month after PCI

Secondary

MeasureTime frame
All cause death MACEE: acute myocardial infarction, stable or unstable angina, any coronary revascularization procedure, or cerebrovascular accident

Countries

Japan

Contacts

Public ContactShun Kohsaka

Keio University, School of Medicine Division of Cardiology

sk@keio.jp03-3353-1211

Outcome results

None listed

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