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Completed

NCT Number: NCT00501423

Antiplatelet Drug Resistances and Ischemic Events

The ADRIE study is an observational study on the clinical relevance of platelet reactivity in aspirin and clopidogrel treated cardiovascular patients.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital Geneva; Beziers and Monpellier University Hospitals, France

Geneva - Beziers - Montpellier, France

About this study

The ADRIE study is an observational study on the clinical relevance of platelet reactivity in aspirin and clopidogrel treated cardiovascular patients.

Main objective:

  • to determine if platelet reactivity, assessed by specific and non-specific tests, is predictive of ischemic events during the 3-year follow-up.

Secondary objectives:

  • primary outcome in each pre-specified sub-group : patients with coronary artery disease, ischemic stroke or peripheral arterial disease as main qualifying disease at entry,
  • to determine if platelet reactivity, assessed by specific and non-specific tests, is predictive of bleeding events during the 3-year follow-up,
  • to investigate potential determinants of platelet reactivity at entry in the study

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Documented symptomatic ischemic atherothrombotic disease treated by aspirin, clopidogrel or both.

Exclusion criteria

  • Known platelet disorder
  • Chronic treatment by antiplatelet drugs other than aspirin or clopidogrel.
  • Chronic anticoagulant treatment
  • Chronic non steroid anti inflammatory drug treatment
  • Active cancer
  • Ongoing aspirin or clopidogrel treatment taken for more than 5 years prior to inclusion

Treatment and study plan

Primary outcomes

  1. MACE

    Time frame: prospective follow-up

    adjudicating committee

Secondary outcomes

  1. MACE in pre-specified sub-groups

    Time frame: prospective follow-up

    patients with coronary artery disease, ischemic stroke or peripheral arterial disease as main qualifying disease at entry

Other outcomes

  1. potential determinants of platelet reactivity

    Time frame: at inclusion

Sponsors and collaborators

Lead sponsor

Pierre Fontana

Other

Collaborators

  • Beziers Hospital
  • Ministry of Health, France
  • Swiss National Science Foundation
  • University Hospital, Montpellier

Registry information

Acronym: ADRIE

Important dates

Study start
2006
Primary completion
2010
Study completion
2010
First posted
Jul 16, 2007
Registry last updated
Jan 31, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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