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Triple Versus Dual Antiplatelet Therapy in Patients Undergoing Coronary Stent Implantation

Primary Purpose

Acute Coronary Syndrome

Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Cilostazol
Sponsored by
Shenyang Northern Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Coronary Syndrome

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosed with ACS Undergoing coronary stent implantation
  • Between ages of above 18 Years and bellow 80 Years.
  • Presence of one or several stenosis in native coronary arteries requiring PCI.
  • Willing and able to sign informed consent.

Exclusion Criteria:

  • A history of bleeding diathesis.
  • New York Heart Association functional class IV.
  • Prior PCI or coronary bypass grafting < 3 months.
  • Contraindications to clopidogrel and aspirin (White blood cells counts < 4×109/L or platelet counts <100 g.l-1 ;creatinine clearance <25 ml • min-1 ;active liver disease).
  • Use of glycoprotein IIb/IIIa inhibitors before PCI.
  • Preparing to undergo CABG
  • Taken clopidogrel or cilostazol recently

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Secondary Outcome Measures

    Full Information

    First Posted
    November 28, 2006
    Last Updated
    November 28, 2006
    Sponsor
    Shenyang Northern Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00404716
    Brief Title
    Triple Versus Dual Antiplatelet Therapy in Patients Undergoing Coronary Stent Implantation
    Official Title
    Effects of Triple Versus Dual Antiplatelet Therapy in Patients With Acute Coronary Syndrome Undergoing Coronary Stent Implantation
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2006
    Overall Recruitment Status
    Completed
    Study Start Date
    December 2004 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    February 2007 (undefined)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Shenyang Northern Hospital

    4. Oversight

    5. Study Description

    Brief Summary
    Cilostazol is an kind of oral antiplatelet agent with a rapid onset of action that selectively inhibits phosphodiesterase III, a mechanism different from adenosine diphosphate (ADP) receptor antagonists. Previous studies had suggested that cilostazol has lipid-modifying and vasodilating effects in addition to antiplatelet effects. From those experimental and clinical backgrounds, we assumed that triple antiplatelet therapy with aspirin, clopidogrel, and cilostazol might have a beneficial effect on the prevention of atherothrombosis complications following coronary stenting. Therefore, we evaluated the safety and efficacy of triple antiplatelet regimen of aspirin, clopidogrel and cilostazol compared with dual antiplatelet regimen of aspirin and clopidogrel in patients with acute coronary syndrome undergoing successful coronary artery stenting. Patients undergoing successful coronary stenting were divided into dual antiplatelet therapy (aspirin plus clopidogrel) and triple antiplatelet therapy (aspirin and clopidogrel plus cilostazol) groups. All enrolled patients in triple regimen group will receive cilostazol 100mg, b.i.d., for 6 months in addition to standard dose and duration of aspirin and clopidogrel for post-PCI. The primary endpoints included death, myocardial infarction, target lesion revascularization, stent thrombosis within 30 days, binary restenosis at six month and major adverse cardiac events (MACE) at one year. The secondary endpoints were side effects of study drugs, including major bleeding, vascular complication, hypersensitivebility, and bleeding complications. The study will be powered to test the hypothesis that triple antiplatelet therapy is better than dual antiplatelet therapy.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Acute Coronary Syndrome

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    Cilostazol

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Diagnosed with ACS Undergoing coronary stent implantation Between ages of above 18 Years and bellow 80 Years. Presence of one or several stenosis in native coronary arteries requiring PCI. Willing and able to sign informed consent. Exclusion Criteria: A history of bleeding diathesis. New York Heart Association functional class IV. Prior PCI or coronary bypass grafting < 3 months. Contraindications to clopidogrel and aspirin (White blood cells counts < 4×109/L or platelet counts <100 g.l-1 ;creatinine clearance <25 ml • min-1 ;active liver disease). Use of glycoprotein IIb/IIIa inhibitors before PCI. Preparing to undergo CABG Taken clopidogrel or cilostazol recently
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Yaling Han, Dr.
    Organizational Affiliation
    Shenyang Northern Hospital
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Triple Versus Dual Antiplatelet Therapy in Patients Undergoing Coronary Stent Implantation

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