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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
Hospital Central San Luis Potosi, Mexico
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Coronary Syndrome focused on measuring Acute Coronary Syndrome, Clopidogrel, Platelet reactivity

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    December 9, 2015
    Last Updated
    December 9, 2015
    Sponsor
    Hospital Central San Luis Potosi, Mexico
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    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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