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

About this trial
This is an interventional treatment trial for Acute Coronary Syndrome
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
Sites / Locations
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00404716
First Posted
November 28, 2006
Last Updated
November 28, 2006
Sponsor
Shenyang Northern Hospital
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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