Effects of Low-dose Ticagrelor vs. Clopidogrel in Stable Patients Undergoing Elective Percutaneous Coronary Intervention

Last updated: April 22, 2025
Sponsor: University of Florida
Overall Status: Active - Recruiting

Phase

4

Condition

Coronary Artery Disease

Hypercholesterolemia

Vascular Diseases

Treatment

Clopidogrel

Ticagrelor 60mg

Clinical Study ID

NCT06228456
IRB202302083
  • Ages > 18
  • All Genders

Study Summary

The proposed study aims to assess the antiplatelet effects of more potent oral P2Y12 inhibition with low-dose ticagrelor (60 mg bid) compared with standard of care clopidogrel in patients with a high ABCD-GENE score (≥10). We hypothesize that ticagrelor is associated with better pharmacodynamic effects (i.e., lower platelet reactivity and high platelet reactivity rates) compared with clopidogrel in stable coronary artery disease patients undergoing percutaneous coronary intervention with a high ABCD-GENE score.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Stable CAD undergoing elective PCI;

  2. Male or females, Age ≥ 18 years old;

  3. Troponin negative before coronary angiography;

  4. On treatment with low-dose aspirin (81mg od) and clopidogrel for at least 24 hoursafter index PCI;

  5. ABCD-GENE score greater or equal than 10.

Troponin negative is defined as hs-cTn below the URL for the laboratory (Male < 22 ng/L; Female < 14 ng/L) or modestly positive hs-cTn (Male: 22-99 ng/L; Female: 14-99 ng/L) flat or decreasing from hour 0 to 3.

Exclusion

Exclusion Criteria:

  1. Myocardial infarction at the time of index PCI;

  2. On treatment with prasugrel or ticagrelor;

  3. Documented hypersensitivity to clopidogrel;

  4. Use of an intravenous antiplatelet therapy (i.e., cangrelor or GPI) in the prior 24hours;

  5. Concomitant therapy with strong CYP3A4 inhibitors or CYP3A4 substrates;

  6. Use of oral anticoagulant therapy;

  7. History of previous intracerebral bleed at any time;

  8. Active pathological bleeding;

  9. Documented hypersensitivity to ticagrelor;

  10. Increased risk of bradycardic events (e.g., known sick sinus syndrome, second orthird degree AV block or previous documented syncope suspected to be due tobradycardia) unless treated with a pacemaker;

  11. Known severe liver disease;

  12. Known platelet count <80x106/mL;

  13. Known hemoglobin <9 g/dL;

  14. Women of child-bearing potential (i.e., those who are not chemically or surgicallysterilized or who are not post-menopause) who are not willing to use a medicallyaccepted method of contraception that is considered reliable in the judgment of theinvestigator OR who have a positive pregnancy test at enrollment or randomization ORwomen who are breast-feeding.

  15. Inability to provide written informed consent.

Study Design

Total Participants: 50
Treatment Group(s): 2
Primary Treatment: Clopidogrel
Phase: 4
Study Start date:
April 01, 2024
Estimated Completion Date:
April 30, 2026

Study Description

Clopidogrel is the P2Y12 inhibitor of choice in patients with stable coronary artery disease (CAD) undergoing elective percutaneous coronary intervention (PCI). However, clopidogrel effects are subject to variability and 30-40% of patients have high platelet reactivity (HPR), which translates into higher rates of thrombotic complications. Despite the relative safety of PCI with new generation stents, peri-PCI thrombotic complications, including myocardial infarction and myocardial injury, are common in elective PCI. Importantly, these events are associated with poor prognosis, including cardiovascular mortality. The risk of peri-PCI myocardial infarction/myocardial injury has been in part attributed to HPR. A precision medicine tool integrating clinical (age, body mass index, chronic kidney disease and diabetes) and genetic (CYP2C19 loss-of-function allele status) factors called ABCD-GENE is able to identify HPR status. This score helps characterize patients at risk for peri-PCI thrombotic complications, who can thus potentially benefit from changes in antiplatelet treatment regimen. The new generation oral P2Y12 inhibitors prasugrel and ticagrelor are more potent than clopidogrel and associated with lower HPR rates and improved outcomes. Hence, these agents may be beneficial in reducing peri-PCI myocardial infarction/myocardial injury. Standard-dose ticagrelor (90 mg bid) provides more potent antiplatelet effect than clopidogrel in patients with ACS. Low-dose ticagrelor (60 mg bid) is beneficial in patients with prior myocardial infarction and has the potential of better bleeding profile compared to standard dose.This prospective randomized study aims to assess the antiplatelet effects of more potent oral P2Y12 inhibition with low-dose ticagrelor (60 mg bid) compared with standard of care clopidogrel in patients with a high ABCD-GENE score (≥10). We hypothesize that ticagrelor is associated with better PD effects (i.e., lower platelet reactivity and HPR rates) compared with clopidogrel in stable CAD patients undergoing PCI with a high ABCD-GENE score.

Connect with a study center

  • University of Florida Jacksonville

    Jacksonville, Florida 32209
    United States

    Active - Recruiting

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.