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The Antiaggregation Monitoring (TAM) Registry

S

Stephane Cook

Status

Completed

Conditions

Aspirin Causing Adverse Effects in Therapeutic Use

Treatments

Other: Measurement of platelet anti-aggregation

Study type

Observational

Funder types

Other

Identifiers

NCT01329224
242/10A

Details and patient eligibility

About

The purpose of this study is to investigate the incidence of acetylsalicylic acid resistance (ASA-R) among patients under chronic acetylsalicylic acid(ASA) treatment seen at our outpatient clinic.

Full description

Acetylsalicylic acid (ASA) resistance (R) is best defined as an ineffective inhibition of the platelet cyclooxygenase (COX)-1 pathway, and has been reported in 1 to 61 % of patients treated with ASA. Impaired response to ASA has been associated with an increased risk of ischemic events in patients with known coronary artery disease. We sought to investigate the incidence of ASA-R in clinical practice.

All consecutive patients under chronic ASA treatment (100mg/d) seen at our outpatient clinic were systematically included in the registry. All patients were on acetylsalicylic acid for CAD for at least 1 month. Patients were informed of ASA testing at start of consultation in the outpatient clinic. Eligible patients provided written informed consent. Peripheral venous blood samples were analyzed using the whole blood impedance platelet aggregometry Multiplate analyzer. The Multiplate analyzer device allows to measure platelet aggregation by the attachment of platelets to two silver coated copper electrodes leading to a rise of electrical resistance in the sample. The measurements are expressed as arbitrary aggregation units (AU) and the manufacturers defined cutoffs were used: normal values were 76-136 AU, partial antiaggregation was defined as ASA values between 31 and 75 AU and complete antiaggregation was defined as ASA values < 31 AU.

Enrollment

200 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients under chronic ASA treatment for more then one month

Exclusion criteria

  • concomitant use of nonsteroidal anti-inflammatory drugs (NSAIDs)
  • thrombocytopenia
  • thrombocytosis
  • age <18 years

Trial design

200 participants in 1 patient group

TAM patients
Description:
All consecutive patients under chronic ASA treatment (100mg/d) seen at our outpatient clinic.
Treatment:
Other: Measurement of platelet anti-aggregation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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