Effect of Amlodipine on Anti-platelet Drug Effect in Patients With Coronary Artery Disease
Primary Purpose
Ischemic Heart Disease
Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Amlodipine
Amlodipine
Sponsored by
About this trial
This is an interventional treatment trial for Ischemic Heart Disease focused on measuring Clopidogrel, Platelet reactivity, Amlodipine
Eligibility Criteria
Inclusion Criteria:
- ischemic heart disease patient, and
- given loading or maintenance dose of clopidogrel and in need of it for 1 or more month
- and in need of additional drug for optimal BP control (aim blood pressure <130/90) or angina control.
Exclusion Criteria:
- existing use of amlodipine
- thrombocytopenia
- end stage renal failure
- allergy to clopidogrel/ amlodipine
- pregnancy/ lactation
- strong inhibitor or inducer of cytochrome P450 3A4 enzyme within 7 days before start of the study.
Sites / Locations
- Ruttonjee Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
non-amlodipine
non - amlodipine
Arm Description
For patient with suboptimal angina control: anti-anginal agent excluding calcium channel blocker
For patient with suboptimal BP control: anti-hypertensive agent excluding calcium channel blocker
Outcomes
Primary Outcome Measures
Platelet reactivity unit
Platelet reactivity unit as measured by VerifyNow system
Secondary Outcome Measures
Percentage inhibition of platelet activity
Percentage inhibition of platelet activity measured by VerifyNow system
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01203696
Brief Title
Effect of Amlodipine on Anti-platelet Drug Effect in Patients With Coronary Artery Disease
Official Title
Effect of Amlodipine on Platelet Inhibition by Clopidogrel in Patients With Ischemic Heart Disease- a Prospective Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
June 2012
Overall Recruitment Status
Completed
Study Start Date
July 2010 (undefined)
Primary Completion Date
April 2011 (Actual)
Study Completion Date
April 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ruttonjee Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Clopidogrel can reduce risk of cardiovascular disease by inhibiting platelet aggregation. It is metabolized to an active drug by a liver enzyme. Its efficacy may be measured by blood sampling for platelet activity, analyzed by VerifyNow device. Calcium Channel blocker (CCB) is also commonly used for blood pressure and anginal control in these patients. Dihydropyridine group of calcium channel blocker (e.g. amlodipine) inhibits this enzyme. There are observational studies reporting dihydropyridine CCB reducing clopidogrel effect, but the clinical implication is unclear.
This study test the hypothesis that there is no significant effect of dihydropyridines CCB on clopidogrel response compared with control. After giving consent, patients with suboptimal blood pressure or anginal control will be randomized to receive either dihydropyridine CCB or non-CCB as placebo. These patient will be follow-up in 1 month.
Detailed Description
Clopidogrel is a pro-drug, which requires hepatic transformation by the cytochrome P450 isoform 3A4 to generate the active metabolite. It inhibits adenosine-5-diphosphate (ADP)-induced platelet aggregation by irreversibly blocking the platelet P2Y12 receptor. However, response to clopidogrel shows wide individual variability, and patients with high on-treatment residual ADP-induced platelet reactivity are at an increased risk of adverse cardiovascular events. Previous study suggest co-administration of CCBs is associated with decreased platelet inhibition by clopidogrel, but these observational studies are confounded by patient's characteristics baseline difference such as proportion of hypertension and diabetes.
The objective of this randomized controlled study is to compare amlodipine with placebo on anti-platelet effect of clopidogrel.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemic Heart Disease
Keywords
Clopidogrel, Platelet reactivity, Amlodipine
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
97 (Actual)
8. Arms, Groups, and Interventions
Arm Title
non-amlodipine
Arm Type
Active Comparator
Arm Description
For patient with suboptimal angina control: anti-anginal agent excluding calcium channel blocker
Arm Title
non - amlodipine
Arm Type
Active Comparator
Arm Description
For patient with suboptimal BP control: anti-hypertensive agent excluding calcium channel blocker
Intervention Type
Drug
Intervention Name(s)
Amlodipine
Other Intervention Name(s)
Norvasc
Intervention Description
For patient with suboptimal angina control: oral 2.5-10mg daily
Intervention Type
Drug
Intervention Name(s)
Amlodipine
Other Intervention Name(s)
Norvasc
Intervention Description
For patient with suboptimal BP control: 2.5-10mg daily po
Primary Outcome Measure Information:
Title
Platelet reactivity unit
Description
Platelet reactivity unit as measured by VerifyNow system
Time Frame
baseline and 4 th week
Secondary Outcome Measure Information:
Title
Percentage inhibition of platelet activity
Description
Percentage inhibition of platelet activity measured by VerifyNow system
Time Frame
baseline and 4th week
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
ischemic heart disease patient, and
given loading or maintenance dose of clopidogrel and in need of it for 1 or more month
and in need of additional drug for optimal BP control (aim blood pressure <130/90) or angina control.
Exclusion Criteria:
existing use of amlodipine
thrombocytopenia
end stage renal failure
allergy to clopidogrel/ amlodipine
pregnancy/ lactation
strong inhibitor or inducer of cytochrome P450 3A4 enzyme within 7 days before start of the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrew YW Li, MB
Organizational Affiliation
Ruttonjee Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ruttonjee Hospital
City
Hong Kong SAR
Country
China
12. IPD Sharing Statement
Citations:
PubMed Identifier
23118347
Citation
Li AY, Ng FH, Chan FK, Tunggal P, Chan K, Lau YK. Effect of amlodipine on platelet inhibition by clopidogrel in patients with ischaemic heart disease: a randomised, controlled trial. Heart. 2013 Apr;99(7):468-73. doi: 10.1136/heartjnl-2012-302801. Epub 2012 Oct 31.
Results Reference
derived
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Effect of Amlodipine on Anti-platelet Drug Effect in Patients With Coronary Artery Disease
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