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Completed

NCT Number: NCT01248351

Reversibility of Dual Antiplatelet Therapy by Platelets

The objective of the study is to test the hypothesis whether or not autologous stored platelets are able to offset the antiplatelet effect of aspirin and clopidogrel as assessed by state-of-the-art platelet function assays.

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Key information

Age range

18 year–30 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Department of anesthesia and intensive care medicine, Medical Univerity of Graz

Graz, 8036, Austria

About this study

Dual antiplatelet therapy with aspirin and clopidogrel is a well established strategy to prevent thrombotic complications in patients with high platelet reactivity following plaque rupture in acute coronary syndromes (ACS) or percutaneous coronary interventions. Current practice guidelines for antiplatelet therapy advocate a one to 12 months dual antiplatelet therapy after bare metal stent PCI and a 12 months dual antiplatelet therapy after PCI in patients with ACS and drug eluting stent PCI. Although oral antiplatelet therapy is associated with both, short- as well as long-term clinical efficacy, irreversible platelet inhibition carries a substantial risk of bleeding particularly in patients presenting for surgery. Empiric therapy of bleeding consists of platelet transfusion. However, there are currently no pharmacodynamic studies assessing the effect of stored platelets on in-vitro platelet function tests.

Healthy volunteers will donate platelets, take aspirin and clopidogrel for 3 days (loading dose aspirin 300 mg, clopidogrel 300 mg, maintenance dose aspirin 100 mg, clopidogrel 75 mg) and platelets will be retransfused on the 4th day. Pharmacodynamic measurements of platelet function will be performed at baseline, after drug intake before retransfusion, immediately after retransfusion and 24 hours thereafter.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Informed consent
  • Healthy volunteers, male or female (after exclusion of pregnancy if they are on birth control pill or have a contraceptive coil implanted)
  • Age of consent
  • Weight: 70 kg - 100 kg
  • Platelet count 240 000 to 440 000/µL
  • Hematocrit > 40%
  • readiness to refrain from any activities prone to injury during the study period.

Exclusion criteria

  • Allergy against aspirin or clopidogrel
  • History of bleeding
  • History of peptic ulcer
  • Intake of aspirin or NSAR during the last ten days before screening
  • Gastrointestinal disease precluding resorption of aspirin and clopidogrel
  • Scheduled surgery
  • Any current medication
  • History of hepatic disease
  • 20µm ADP induced aggregation < 60% at screening
  • CYP2C19 polymorphisms
  • Donation of blood within the preceding 4 weeks
  • Neurotic disease
  • Current smoking
  • Drug addiction
  • Intake of grapefruits during the last 10 days before

Treatment and study plan

autologous stored platelets

Other

Administration of autologous stored platelets

administration of autologous stored platelets

Other

administration of autologous stored platelets

autologous stored platelets

Biological

transfusion of autologous stored platelets

Primary outcomes

  1. Pharmacodynamic assessment of platelet function as assessed by 5 and 20 micromolar ADP

    Time frame: 7 days

    pharmacodynamic measurements of platelet function will be assessed at baseline, after 3 days administration of aspirin and clopidogrel (300 mg loading with aspirin and clopidogrel, maintenance with 100 mg aspirin and 75 mg clopidogrel, respectively) after retransfusion of stored platelets and 24 hours thereafter

Secondary outcomes

  1. Pharmacodynamic assessment of platelet function as assessed by 20 mM arachidonic acid

    Time frame: 7 days

    pharmacodynamic measurements of platelet function will be assessed at baseline, after 3 days administration of aspirin and clopidogrel (300 mg loading with aspirin and clopidogrel, maintenance with 100 mg aspirin and 75 mg clopidogrel, respectively) after retransfusion of stored platelets and 24 hours thereafter

  2. Pharmacodynamic assessment of platelet function as assessed by Vasodilator stimulated phosphoprotein (VASP) phosphorylation (platelet reactivity index; PRI)

    Time frame: 7 days

    pharmacodynamic measurements of platelet function will be assessed at baseline, after 3 days administration of aspirin and clopidogrel (300 mg loading with aspirin and clopidogrel, maintenance with 100 mg aspirin and 75 mg clopidogrel, respectively) after retransfusion of stored platelets and 24 hours thereafter

  3. Pharmacodynamic assessment of platelet function as assessed by expression of GP IIb/IIIa receptors and P-selectin (Mean fluorescence intensity %)

    Time frame: 7 days

    pharmacodynamic measurements of platelet function will be assessed at baseline, after 3 days administration of aspirin and clopidogrel (300 mg loading with aspirin and clopidogrel, maintenance with 100 mg aspirin and 75 mg clopidogrel, respectively) after retransfusion of stored platelets and 24 hours thereafter

Sponsors and collaborators

Lead sponsor

Medical University of Graz

Other

Collaborators

  • CSL Behring
  • Novo Nordisk A/S

Registry information

Official study title

Reversibility of Dual Antiplatelet Therapy by Platelets.Phase II Study

Important dates

Study start
2010
Primary completion
2011
Study completion
2011
First posted
Nov 25, 2010
Registry last updated
Apr 28, 2011

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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