The ACS Ethnicity Platelet Function Study

• ClinicalTrials.gov Identifier: NCT01829659
• Recruitment Status: Completed
• First Posted: April 11, 2013
• Last Update Posted: June 8, 2018
• Sponsor: Medstar Health Research Institute
• Information provided by (Responsible Party): Medstar Health Research Institute

Study Description

Brief Summary:

This study is being done to assess the effects of the CTP inhibitor on the function of your platelets (cells within your blood that are involved in the formation of blood clots) and to assess whether you have responded to the ticagrelor well enough to prevent the formation of blood clots within the stent or site in which angioplasty was performed.

Recent studies have looked at how racial differences can affect platelet reactivity, the way blood clots. But these studies have not looked at the way different racial backgrounds can affect the way the blood forms clots. Minorities, such as African-Americans are underrepresented. Therefore, we are conducting this platelet reactivity study to better understand if there are differences in how this drug affects African-Americans from how they affect Caucasian patients undergoing percutaneous coronary intervention and receiving ticagrelor. These data will be compared to a historical control of Caucasian patients who underwent similar platelet function testing.

Condition or disease	Intervention/treatment
Acute Coronary Syndrome	Drug: Ticagrelor

Study Design

• Study Type: Observational
• Actual Enrollment: 4 participants
• Observational Model: Cohort
• Time Perspective: Prospective
• Official Title: The ACS Ethnicity Platelet Function Study
• Study Start Date: May 2013
• Actual Primary Completion Date: March 2016
• Actual Study Completion Date: May 2016

Groups and Cohorts

Group/Cohort	Intervention/treatment
AA Ticagrelor; African Americans who present with acute coronary syndrome (ACS) to the cath lab, and receive ticagrelor during their hospital stay.	Drug: Ticagrelor

Outcome Measures

Primary Outcome Measures :

1. Ticagrelor Inhibition [ Time Frame: 1-2 days ]
   The primary objective of the study is to assess ticagrelor's inhibition of platelet activity using 3 assays simultaneously: VerifyNow P2Y12 (PRU), vasodilator-stimulated phosphoprotein phosphorylation (VASP) and light transmission aggregometry (LTA) in African-American patients presenting with ACS.

Secondary Outcome Measures :

1. Follow-up Adverse Events [ Time Frame: 30 days ]
   To evaluate the safety of ticagrelor treatment in African-American patients by assessment of adverse-events up to 30-day follow-up time point.

Eligibility Criteria

• Ages Eligible for Study: 18 Years and older (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No
• Sampling Method: Non-Probability Sample

Study Population

Thirty African American patients with documented acute coronary syndrome who agree to participate in this clinical study and who sign an informed consent will be enrolled.

Race determination will be based on a patient's self-report, but patients enrolled in the trial must also report that all four of their grandparents were of the same race as theirs. Other races (Asian, Native American, etc) will be excluded from this study.

Criteria

Inclusion Criteria:

• Female (post menopausal or surgically sterile) and/or male aged 18 years or older

• Presenting with ACS fulfilling the following:

  1. Symptoms or new ECG changes (ST segment elevation or depression of at least 1 mm in 2 or more contiguous leads on EKG)
  2. Elevation of biomarkers (CK-MB ≥2 ULN or troponin ≥ ULN)
• Self-identified as African-American
• Treatment with 75-100mg ASA daily

Exclusion Criteria:

• Any indication (atrial fibrillation, mitral stenosis or prosthetic heart valve, PE, DVT) for antithrombotic treatment during study period.
• Fibrinolytic therapy within 48 hours before randomization
• Concomitant therapy with a drug having possible interaction with ticagrelor. (concomitant therapy with a strong cytochrome P-450 3A inhibitor or inducer)
• Increased bleeding risk including: recent (<30 days) GI bleeding, any history of intracranial, intraocular, retroperitoneal, or spinal bleeding, recent (<30 days of dosing) major trauma, sustained uncontrolled hypertension (systolic blood pressure [SBP]>180mmHg or diastolic blood pressure [DBP]>100mmHg), history of hemorrhagic disorders that can increase the risk of bleeding, platelet count less than 100,000 mm3 or hemoglobin <10 g/dL.
• Any history of hemorrhagic stroke.
• Contraindication or other reason that ASA or ticagrelor should not be administered (e.g., hypersensitivity, active bleeding, major surgery within 30 days of dosing).
• Severe renal failure (creatinine clearance <30mL/min or patient requires dialysis)
• History of moderate or severe hepatic impairment with aspartate amino transferace, alanine amino transferase or total bilirubin > 1.5 x upper limit of the reference range.
• Pregnant or lactating women.
• Patients receiving any glycoprotein IIb/IIIa inhibitors <8 hours before platelet reactivity testing.

Contacts and Locations

Locations

United States, District of Columbia

Medstar Washington Hospital Center

Washington, District of Columbia, United States, 20010

Sponsors and Collaborators

Medstar Health Research Institute

Investigators

• Principal Investigator: Ron Waksman, MD; Medstar Washington Hospital Center

More Information

• Responsible Party: Medstar Health Research Institute
• ClinicalTrials.gov Identifier: NCT01829659
• Other Study ID Numbers: ACS Brilinta AZ
• First Posted: April 11, 2013
• Last Update Posted: June 8, 2018
• Last Verified: June 2018

Additional relevant MeSH terms:

Acute Coronary Syndrome; Myocardial Ischemia; Heart Diseases; Cardiovascular Diseases; Vascular Diseases; Ticagrelor; Platelet Aggregation Inhibitors; Purinergic P2Y Receptor Antagonists; Purinergic P2 Receptor Antagonists; Purinergic Antagonists; Purinergic Agents; Neurotransmitter Agents; Molecular Mechanisms of Pharmacological Action; Physiological Effects of Drugs