Patent Versus Generic Clopidogrel in Acute Coronary Syndrome
Primary Purpose
Acute Coronary Syndrome
Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Generic clopidogrel
Patent clopidogrel
Sponsored by
About this trial
This is an interventional treatment trial for Acute Coronary Syndrome focused on measuring Acute Coronary Syndrome, Clopidogrel, Platelet reactivity
Eligibility Criteria
Inclusion Criteria:
- 18 and over
- Diagnosis of acute coronary syndrome
- Patients receiving 300 mg of Clopidogrel load and a single dose of 75 mg daily
- Signature of informed consent
Exclusion Criteria:
- Active bleeding or absolute contraindication for antiplatelet use
- Chronic kidney disease with creatinine clearance <30 ml / min
- Liver damage documented as elevated aspartate aminotransferase/alanine aspartate 2 times upper normal limit (UNL) and/or total bilirubin > 2 times UNL
- Prescribed antiplatelet therapy, other than aspirin
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Generic clopidogrel
Patent clopidogrel
Arm Description
Patients are assigned to take generic clopidogrel
Patients are assigned to take patent clopidogrel (Plavix)
Outcomes
Primary Outcome Measures
Platelet reactivity change
Change in platelet reactivity measured from day 0 to day 3 of Clopidogrel therapy
Secondary Outcome Measures
Full Information
NCT ID
NCT02628587
First Posted
December 9, 2015
Last Updated
December 9, 2015
Sponsor
Hospital Central San Luis Potosi, Mexico
1. Study Identification
Unique Protocol Identification Number
NCT02628587
Brief Title
Patent Versus Generic Clopidogrel in Acute Coronary Syndrome
Official Title
Comparison of Platelet Reactivity in Patients With Acute Coronary Syndrome Given Patent Clopidogrel Versus Generic Clopidogrel: Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
December 2015
Overall Recruitment Status
Unknown status
Study Start Date
February 2016 (undefined)
Primary Completion Date
June 2016 (Anticipated)
Study Completion Date
June 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Central San Luis Potosi, Mexico
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Ischemic heart disease is the leading cause of death and disability in developed countries and is responsible for a third of deaths in persons over 35 years . The most severe form of ischemic heart disease is sudden death and acute coronary syndrome (ACS).
There is evidence that early and optimal treatment of ACS decreases mortality. Within the optimal treatment, these patients must receive a reperfusion therapy as mechanical or pharmacologic treatment. In addition to reperfusion treatment, antiplatelet therapy is a central part of the management. Aspirin plus a P2Y12 inhibitor have been shown to decrease mortality. In our country, clopidogrel is the more accessible and used P2Y12 inhibitor; however, it has been shown to have a wide variability in response and this variability could be influenced by different pharmacological, genetic and environmental factors.
Platelet reactivity measured by aggregometry predicts major cardiovascular events in ACS patients treated with clopidogrel. Due to their frequent prescription, generic clopidogrel efficacy must be evaluated. The purpose of this study is to compare the platelet reactivity in patients with ACS receiving clopidogrel generic versus patent.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Coronary Syndrome
Keywords
Acute Coronary Syndrome, Clopidogrel, Platelet reactivity
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Generic clopidogrel
Arm Type
Experimental
Arm Description
Patients are assigned to take generic clopidogrel
Arm Title
Patent clopidogrel
Arm Type
Active Comparator
Arm Description
Patients are assigned to take patent clopidogrel (Plavix)
Intervention Type
Drug
Intervention Name(s)
Generic clopidogrel
Intervention Description
Comparison of different brands of clopidogrel:
*Clopidogrel (generic) 300mg orally single dose on day 0. Later, clopidogrel 75mg orally single dose on days 1, 2 and 3.
Intervention Type
Drug
Intervention Name(s)
Patent clopidogrel
Other Intervention Name(s)
Plavix
Intervention Description
Comparison of different brands of clopidogrel:
*Clopidogrel (Plavix) 300mg orally single dose on day 0. Later, clopidogrel 75mg orally single dose on days 1, 2 and 3.
Primary Outcome Measure Information:
Title
Platelet reactivity change
Description
Change in platelet reactivity measured from day 0 to day 3 of Clopidogrel therapy
Time Frame
Day 0 and Day 3
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 and over
Diagnosis of acute coronary syndrome
Patients receiving 300 mg of Clopidogrel load and a single dose of 75 mg daily
Signature of informed consent
Exclusion Criteria:
Active bleeding or absolute contraindication for antiplatelet use
Chronic kidney disease with creatinine clearance <30 ml / min
Liver damage documented as elevated aspartate aminotransferase/alanine aspartate 2 times upper normal limit (UNL) and/or total bilirubin > 2 times UNL
Prescribed antiplatelet therapy, other than aspirin
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Patent Versus Generic Clopidogrel in Acute Coronary Syndrome
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