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Trials / Completed

CompletedNCT01039480

Aspirin and Clopidogrel Resistance Study

Aspirin- and Clopidogrel-Resistance: Non-compliance and Other Contributing Factors

Status
Completed
Phase
Study type
Observational
Enrollment
82 (actual)
Sponsor
University Hospital, Basel, Switzerland · Academic / Other
Sex
All
Age
45 Years
Healthy volunteers
Not accepted

Summary

Resistance to antiplatelet drugs (aspirin, clopidogrel) is a recognized phenomenon with a prevalence from 17% to 35%. Resistance as detected by in vitro tests such as Multiple Electrode Aggregometry (MEA) has been shown to predict clinical therapy failure. Resistance can be caused by clinical, cellular and pharmacogenetic factors. Non compliance is suspected to be an important contributing factor. In this study, compliance will be assured with an electronical compliance monitoring system. Factors to non response will be identified to find plausible explanations when in vitro platelet aggregation inhibition is insufficient despite assured compliance. This study will help to disclose the relationship between compliance, biomarker and clinical outcome as well as to quantify the impact of non compliance to the resistance phenomenon as measured by MEA.

Conditions

Timeline

Start date
2010-05-01
Primary completion
2011-06-01
Completion
2011-10-01
First posted
2009-12-25
Last updated
2012-02-09

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT01039480. Inclusion in this directory is not an endorsement.

Aspirin and Clopidogrel Resistance Study (NCT01039480) · Clinical Trials Directory