Acute Coronary Syndrome Clinical Trial
Official title:
Aspirin Impact on Platelet Reactivity in Acute Coronary Syndrome Patients on Novel P2Y12 Inhibitors Therapy
| Verified date | February 2018 |
| Source | Sheba Medical Center |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Thus far, no study has evaluated the impact on aspirin in addition to the newer and more
potent P2Y12 inhibitors, among ACS patients and current guidelines recommend dual
anti-platelet therapy consisting of aspirin and a novel P2Y12 inhibitor in this population.
Objective The investigators goal is to examine the effect of aspirin in addition to new
anti-platelet agent (ticagrelor\prasugrel) on platelet reactivity in comparison with placebo,
among ACS patients treated percutaneously.
Design The proposed study is a randomized-controlled, double blind trial, conducted among ACS
patients treated percutaneously. Eligible patients will recruited during hospitalization due
to ACS after percutaneous coronary intervention (PCI), and randomization by envelopes on 1:1
basis will take place a month after the index event, at a follow-up visit at the cardiac
clinic.
Platelet function and Endothelial function tests will be taken a month after the index event,
and at a 2 weeks periods following aspirin/placebo therapy, cross-over and return to
open-label aspirin.
End-points platelet function tests will be compared between aspirin and placebo therapy and
before and after the cross-over.
| Status | Completed |
| Enrollment | 29 |
| Est. completion date | January 2017 |
| Est. primary completion date | January 2017 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 80 Years |
| Eligibility |
Inclusion Criteria: - Age>18 years - ACS defined according to the 3rd universal definition of MI - PCI therapy Exclusion Criteria: - Indication for anticoagulant therapy - ACS on new P2Y12 inhibitors treatment - Contraindication to P2Y12 therapy - Renal failure defined as creatinine =1.5 mg/dL - Non-compliance - Life-threatening extra-cardiac disease or malignancy with a life expectancy below 1 year - Inability to sign an informed consent - Participation in another trial during the previous 6 months |
| Country | Name | City | State |
|---|---|---|---|
| Israel | Sheba Medical Center | Tel-Hashomer |
| Lead Sponsor | Collaborator |
|---|---|
| Sheba Medical Center |
Israel,
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Wallentin L, Becker RC, Budaj A, Cannon CP, Emanuelsson H, Held C, Horrow J, Husted S, James S, Katus H, Mahaffey KW, Scirica BM, Skene A, Steg PG, Storey RF, Harrington RA; PLATO Investigators, Freij A, Thorsén M. Ticagrelor versus clopidogrel in patients with acute coronary syndromes. N Engl J Med. 2009 Sep 10;361(11):1045-57. doi: 10.1056/NEJMoa0904327. Epub 2009 Aug 30. — View Citation
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* Note: There are 14 references in all — Click here to view all references
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Other | clinical outcome | hospitalizations and mortality | two months | |
| Primary | Platelet reactivity | platelet reactivity in response to arachidonic acid | one month | |
| Secondary | platelet reactivity | platelet reactivity in response to ADP | one month |
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