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Effects of ivabradine in patients with coronary artery disease and suffering from a reversible contractility dysfunction of the heart muscle

Not Applicable
Completed
Conditions
Coronary artery disease
Circulatory System
Registration Number
ISRCTN90566768
Lead Sponsor
Institut de Recherches Internationales Servier (France)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
15
Inclusion Criteria

1. Aged 30 to 75 years
2. Male or female
3. Evidence of coronary artery disease proven by clinical history
4. Sinus rhythm and resting heart rate equal or higher than 70 bpm
5. Exercise-inducible myocardial ischaemia
6. Myocardial stunning, assessed by cardiac echocardiography

Exclusion Criteria

1. Angina at rest or angina class IV
2. Unstable cardiovascular condition
3. Previous treament with anti-anginal medication within 1 week before inclusion
4. Significant abnormalities in the laboratory blood evaluation
5. Contra-indication to the administration of ivabradine

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<br> 1. Myocardial stunning, by evaluating changes in regional wall motion measuring 2D Strain/Strain rate<br> 2. Measured at selection visit, inclusion visit and end of treatment visit<br>
Secondary Outcome Measures
NameTimeMethod
<br> 1. Arterial elastance, measured at selection visit, inclusion visit and end of treatment visit<br> 2. Ventricular arterial coupling, measured at selection visit, inclusion visit and end of treatment visit<br> 3. Safety, measured at each visit<br>
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