Danish Aspirin Resistance Trial - Pilot Study
Information source: University of Aarhus
Information obtained from ClinicalTrials.gov on June 20, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Drug Resistance
Intervention: acetylsalicylic acid (Drug)
Phase: N/A
Status: Completed
Sponsored by: University of Aarhus Official(s) and/or principal investigator(s): Steen D Kristensen, MD, DMSc, Study Director, Affiliation: Department of Cardiology, Skejby Sygehus, Aarhus University Hospital, 8200 Aarhus N, DK - Denmark Erik L Grove, MD, Principal Investigator, Affiliation: Department of Cardiology, Skejby Sygehus, Aarhus University Hospital, 8200 Aarhus N, DK - Denmark
Summary
Despite treatment with aspirin a large number of patients suffer a myocardial infarction. It
has been speculated that these patients might be "resistant" to aspirin, and studies have
indicated that this phenomenon is related to a less favourable prognosis. At present, no
international consensus exists on how to measure "aspirin resistance". The purpose of this
study is to compare different methods for detecting "aspirin resistance". A classic but
cumbersome way of evaluating platelet function will be compared to newer, easy-handling
point-of-care tests. We hypothesize that one or more point-of-care tests will prove to be
superior to the classic platelet function test in detecting aspirin resistance.
Clinical Details
Official title: Comparative Evaluation of Aspirin Resistance With Point-of-Care Testing - Danish Aspirin Resistance Trial (DANART) - Pilot Study
Study design: Diagnostic, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Pharmacodynamics Study
Primary outcome: Platelet aggregation (as determined by 3 point-of-care tests and by serum-thromboxane A2 + urine 11-dehydro thromboxane B2) is measured once daily for 4 days after one week of treatment with aspirin 75 mg/day
Detailed description:
Platelets play a major role in arterial thrombus formation - the cause of cardiovascular
death, acute myocardial infarction and ischemic stroke and the number one killer in the
Western World. Binding the COX enzyme platelet aggregation is inhibited by aspirin, and as
prophylaxis against death, myocardial infarction and stroke aspirin is the most widely used
drug worldwide. Low dose aspirin has been shown to improve outcome in patients with ischemic
heart disease, but approximately 12% of these patients will suffer from a vascular event
during a 2 year follow-up period despite aspirin therapy. It has been speculated that these
patients might be "resistant" to the antiaggregatory effect of aspirin, and a diminished
response to aspirin has been correlated with a less favourable outcome. However, at present
no international consensus exists on how to measure "aspirin resistance".
Comparisons: The platelet aggregation in patients with ischemic heart disease on chronic, low
dose aspirin is compared to platelet aggregation i healthy volunteers evaluated with
different tests. The traditional way of evaluating platelet function, Platelet Aggregometry
a. m. Born, will be compared to 3 point-of-care tests (VerifyNow, PFA-100 and Multiplate Whole
Blood Aggregometer) and to urin- and serum thromboxane metabolites as a measure of COX
inhibition.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- ischemic heart disease verified with a coronary angiogram
- treatment with 75 mg aspirin once daily
Exclusion Criteria:
- ischemic vascular event within the previous 12 months
- percutaneous coronary intervention or coronary artery by-pass grafting within the
previous 12 months
- treatment with NSAID, clopidogrel, ticlopidine, dipyridamole, warfarin or any other
drug affecting platelet aggregation
- platelet count < 120 x 10^9/l
- not able to give informed consent
Locations and Contacts
Department of Cardiology, Skejby Sygehus, Aarhus University Hospital, Aarhus 8200, Denmark
Additional Information
Starting date: November 2006
Ending date: March 2007
Last updated: December 10, 2007
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