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Clinical Trials/NCT02201394
NCT02201394
Completed
Phase 4

Normalizing Platelet Reactivity After Treatment With Ticagrelor

Icahn School of Medicine at Mount Sinai1 site in 1 country20 target enrollmentJuly 2014

Overview

Phase
Phase 4
Intervention
Ticagrelor loading dose
Conditions
Coronary Artery Disease
Sponsor
Icahn School of Medicine at Mount Sinai
Enrollment
20
Locations
1
Primary Endpoint
P2Y12 Reaction Unit (PRU)
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Acute coronary syndrome (ACS) patients treated with antiplatelet drugs who require coronary artery bypass grafting (CABG) surgery have to wait 5-7 days for the effects of the drugs to wean off. This treatment-devoid period leaves the patient vulnerable, therefore any means to shorten this period could be useful. The present study aims to investigate the possibility of reversing the antiplatelet effects of ticagrelor with the help of fresh donor platelets. Fresh platelets will be added to blood samples of treated patients in varying concentrations at specific timepoints to determine the time and amount of fresh platelets needed to normalize platelet reactivity in the treated samples.

Detailed Description

The current American College of Cardiology/American Heart Association (ACC/AHA) guidelines for ACS patients requiring CABG surgery after treatment with dual antiplatelet therapy recommend delaying surgery for 5-7 days after discontinuation of therapy, to allow for the dissipation of its antiplatelet effects. This treatment-devoid waiting period puts the ACS patients at risk for further cardiovascular events. Any means to shorten this vulnerable period would be of critical value. One possibility to speed up the recovery of the inhibited platelets is to administer infusions of fresh platelets. In fact, platelet transfusions are frequently administered to patients during surgery who had received prior antiplatelet therapy. However, the degree to which these transfusions restore platelet function in the recipient subjects' blood and the time from dosing when they are most effective are unknown. The timing is critical in scenarios where urgent surgery is required because infusion of platelets too soon after antiplatelet dosing could render them useless by the residual drug in circulation. The aim of the present study is to investigate the restoration of platelet function of ticagrelor-treated subjects by adding donor platelets to their blood. The study would have 2 arms mimicking different clinical scenarios: 1. Clinical Scenario 1 - Patient given a loading dose (LD) of ticagrelor in the emergency room, requires surgery: A single LD of ticagrelor (180 mg) with aspirin (325 mg) will be given to study subjects and platelet testing will be performed after addition of fresh platelets to their blood ex vivo. Donor platelets will be added at 4-, 6-, 24- and 48-hours post-dose, to assess the time required for normalizing subject's platelet function after a LD of ticagrelor. 2. Clinical Scenario 2 - Patient on maintenance dosing (MD) of ticagrelor, requires surgery: Subjects will receive ticagrelor (90 mg twice daily) with aspirin (81 mg once daily) for 3-7 days. After the last dose, platelet testing will be performed after addition of fresh platelets to their blood ex vivo, at 4-, 6-, 24- and 48-hours post-dose to assess the time required for normalizing subject's platelet function after daily treatment with ticagrelor. Platelet testing will be carried out using the following methodologies: 1. Platelet Aggregation - VerifyNow P2Y12 assay. 2. Platelet Aggregation - Multiplate Analyzer.

Registry
clinicaltrials.gov
Start Date
July 2014
End Date
June 2016
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Juan J Badimon

Director, AtheroThrombosis Research Unit; Professor of Medicine

Icahn School of Medicine at Mount Sinai

Eligibility Criteria

Inclusion Criteria

  • Male or female volunteer between 18 and 75 years old.
  • History of stable (i.e. non-acute) cardiovascular disease or the presence of risk factors for cardiovascular disease (i.e. hypertension, diabetes, hyperlipidemia, high calcium score and abnormal findings on angiography or stress test).

Exclusion Criteria

  • Conditions associated with hemorrhagic risk, e.g., frequent epistaxis, gastrointestinal ulcer, hemorrhagic vascular lesions, recent surgery.
  • Allergy or hypersensitivity to aspirin or ticagrelor.
  • Loss of \>400 mL blood or blood donation within past 3 months.
  • Positive serology for hepatitis B (HBs Ag) or hepatitis C.
  • History of drug abuse or alcohol abuse.
  • Positive pregnancy test.
  • Evidence of unstable or acute cardiovascular disease (e.g., unstable angina, recent myocardial infarction, congestive heart failure).
  • History of clinically relevant pulmonary, hepatic, gastrointestinal, renal, metabolic, hematologic, neurologic, respiratory or psychiatric disease, bleeding, acute infectious disease or signs of acute illness.

Arms & Interventions

Loading dose

Patients with stable CVD given a single ticagrelor loading dose and aspirin loading dose

Intervention: Ticagrelor loading dose

Loading dose

Patients with stable CVD given a single ticagrelor loading dose and aspirin loading dose

Intervention: Aspirin loading dose

Maintenance dose

Patients with stable CVD given ticagrelor maintenance dose and aspirin maintenance dose for one week.

Intervention: Ticagrelor maintenance dose

Maintenance dose

Patients with stable CVD given ticagrelor maintenance dose and aspirin maintenance dose for one week.

Intervention: Aspirin maintenance dose

Outcomes

Primary Outcomes

P2Y12 Reaction Unit (PRU)

Time Frame: Baseline (pre-treatment), 4, 6, 24 and 48 hours post Loading dose/last Maintenance dose

Platelet function normalization using different concentrations (0%, 25%, 50%, and 75% supplementations) of fresh platelet within 48 hours of Ticagrelor Loading dose/last Maintenance dose, assessed using VerifyNow and expressed as P2Y12 Reaction Unit (PRU). The P2Y12 reaction unit (PRU) is an arbitrary unit of measure that represents the amount of platelet aggregation specific to the P2Y12 receptor.

Platelet Aggregation Using Multiplate Analyzer

Time Frame: Baseline (pre-treatment), 4, 6, 24, and 48 hours post Loading dose/last Maintenance dose

Platelet function normalization using different concentrations of fresh platelet within 48 hours of Ticagrelor Loading dose/last Maintenance dose, assessed using Multiplate Aggregometry (ADPtest), results expressed as Area Under Curve (U), where 1 U = 10 AU \* min.

Study Sites (1)

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