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The ITALIC Study: Is There A LIfe for Drug-Eluting Stents (DES) After Discontinuation of Clopidogrel
This study is not yet open for participant recruitment.
Verified by French Cardiology Society, October 2008
Sponsors and Collaborators: French Cardiology Society
Abbott Vascular
Information provided by: French Cardiology Society
ClinicalTrials.gov Identifier: NCT00780156
  Purpose

Background

Drug-eluting stents (DES) have been extremely successful in reducing restenosis and the need for repeat revascularization procedures in patients who undergo PCI. The potential increased incidence of late stent thrombosis prompted cardiologists to prolong the use of dual anti-platelet therapy after the one year duration recommended by the recent ESC guidelines. However, while the premise that the cardiologists should put all their patients on dual clopidogrel-aspirin regimen for life sounds the easy way, it is an unrealistic goal because of the potential increase of bleeding complications and of the healthcare cost increase. The recent possibility to monitor aspirin with bedside assays offers a real opportunity to compare in good aspirin responder patients the two strategies: aspirin-clopidogrel regimen versus mono-aspirin regimen and to respond to the key question: can we switch from dual to single antiplatelet therapy after six months in good aspirin responder patients ? Study National, multicenter, randomised prospective open group comparison of dual clopidogrel-ASA versus single ASA regimen after six months, in good ASA responder patients treated with DES (name: XIENCE) implantation.

End point Primary: At 12 months: death, myocardial infarction, repeat urgent revascularization, stroke requiring a new hospitalisation and major bleedings.

Secondary: Incidence at 24 and 36 months after drug eluting stent(name: XIENCE) implantation, of the same composite endpoint and incidence at 12, 24 and 36 months of minor bleeding complications Participating centres: 60 french centers

Date of study beginning: November 2008 Duration of inclusion: 9 months Duration of study: 45 months


Condition
Follow-up of the Drug Eluting Stent
Restenosis

Drug Information available for: Clopidogrel Clopidogrel Bisulfate
U.S. FDA Resources
Study Type: Observational
Study Design: Prospective
Official Title: The ITALIC Study Is There A LIfe for DES After Discontinuation of Clopidogrel : The ITALIC Study

Further study details as provided by French Cardiology Society:

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 3200
Study Start Date: November 2008
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

Patients after drug eluting stent implantation

Criteria

Inclusion Criteria:

  • Male or female subject ≥18 years of age eligible for PCI with at least one drug eluting stent (name: Xience) implanted in all clinical situations excluding primary PCI for acute MI and treatment of the left main artery.
  • Male or female subject ≥18 years of age eligible for PCI with at least one DES Xience.
  • Patient not pre-treated with protein IIb/IIIa inhibitors (name: abxicimab or eptifibatide) during hospitalization
  • Patient pre-treated with aspirin and clopidogrel before PCI
  • ASA check at least 24 hours after the interruption of tirofiban
  • The subject has given written informed and dated consent to participate in this study.

Exclusion Criteria:

  • Subjects not able to give informed consent
  • Prior implantation of DES
  • Known platelets< 100 000/µl or known hemorrhagic diathesis
  • Oral anticoagulation or treatment with abxicimab or eptifibatide during hospitalization
  • ASA check less than 24 hours after the interruption of tirofiban
  • Thrombolytic therapy within 4 days before ASA check
  • Contra-indication to aspirin or clopidogrel
  • Recent major surgery <6 weeks
  • Evidence of an active gastrointestinal or urogenital bleeding
  • Severe liver insufficiency
  • Primary PCI for acute MI
  • Left main PCI
  • Any scheduled surgery during the year after enrolment
  • Severe concomitant disease with life expectation < two years
  Contacts and Locations
No Contacts or Locations Provided
  More Information

Responsible Party: GACI ( French Cardiology Society )
Study ID Numbers: 2008-004131-38, 2008-02
Study First Received: October 24, 2008
Last Updated: October 27, 2008
ClinicalTrials.gov Identifier: NCT00780156  
Health Authority: France: Afssaps - French Health Products Safety Agency

Keywords provided by French Cardiology Society:
Drug eluting stent
Dual antiplatelet therapy
bleeding
stent thrombosis

Study placed in the following topic categories:
Clopidogrel
Hemorrhage
Thrombosis

Additional relevant MeSH terms:
Therapeutic Uses
Hematologic Agents
Platelet Aggregation Inhibitors
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 16, 2009