Differential Effect of Ticagrelor Versus Prasugrel Maintenance Dose on Endothelial Function of Peripheral Vessels in Patients With Coronary Artery Disease

University of Patras

Status and phase: Completed; Phase 4

Conditions: Endothelial Function; Coronary Artery Disease

Treatments: Drug: Ticagrelor; Drug: Prasugrel

Study type: Interventional

Funder types: Other

Identifiers

NCT01957540

PATRASCARDIOLOGY-16

Details and patient eligibility

About

Ticagrelor administration, whose molecule resembles to adenosine, led to reduction in overall mortality and thrombotic cardiovascular (CV) events when directly compared to clopidogrel in the PLATO trial, implicating possible pleiotropic actions for the drug. It has been shown that ticagrelor increases adenosine concentration, by interfering with its red blood cells' uptake and by inducing the release of ATP which is then converted to adenosine. Recent studies in healthy volunteers and patients with coronary artery disease (CAD) have shown that ticagrelor increases the coronary blood flow in response to intravenous adenosine administration. Ticagrelor administration, in comparison with other P2Y12 inhibitors, may influence the endothelial function, as assessed by the Peripheral Arterial Tonometry method (EndoPAT 2000 system (Itamar Medical, Caesarea, Israel), which is a method for evaluating endothelial dysfunction and has been found to positively correlate with flow mediated dilatation (FMD).

This is prospective, randomized study with a crossover design, which will be conducted in patients with CAD under prasugrel maintenance dose (MD) 10mg once a day for at least a 3-month period. At Day 0 (day of randomization) eligible patients will be assigned to either:

• Ticagrelor 90mg twice a day for the next 15 days or
• Prasugrel 10mg once a day for the next 15 days At Day 0 (before treatment onset)patients wiil be subjected to a baseline peripheral arterial tonometry measurement. Measurement will be repeated at Day 15 and then treatment crossover will be performed for the next 15 days (without an intervening washout period). At Day 30 patients will be subjected again to peripheral arterial tonometry assessment. Peripheral blood sample will be taken from the patients in Day 0 for genotyping control.

Enrollment: 22 patients

Sex: All

Ages: 18 to 74 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Age 18-74 years old
2. Patients with stable CAD who have been submitted(?) to percutaneous intervention for Acute Coronary Syndrome and receiving prasugrel MD 10mg once a day for at least the previous 3 months.
3. Patients giving written Informed Consent.

Exclusion criteria

1. Acute Coronary Syndrome

2. Contraindication for administration of prasugrel or ticagrelor

   1. Known hypersensitivity to clopidogrel or ticagrelor
   2. Active bleeding (peptic ulcer, intracranial bleeding)
   3. Severe liver impairment
   4. Any previous history of intracranial bleeding or transient ischemic attack or ischemic cerebrovascular event
   5. Treatment with potent CYP3A4 inhibitors (ketoconazole, clarithromycin, nefazodone, ritonavir, atazanavir)

3. Requirement for oral anticoagulant agents prior to the day 30 visit

4. History of gastrointestinal bleeding, genitourinary bleeding or other site abnormal bleeding within the previous 3 months

5. Increased risk for bradyarrhythmias, according to the investigator's evaluation

6. Severe non-controlled chronic obstructive pulmonary disease

7. Creatinine clearance <30ml/min/1.73mm2

8. HbA1c > 10mg/dl

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Single Blind

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22 participants in 2 patient groups

Ticagrelor

Experimental group

Description:

Ticagrelor 90mg bid for 15 days

Treatment:

Drug: Ticagrelor

Drug: Prasugrel

Prasugrel

Active Comparator group

Description:

Prasugrel 10mg od for 15 days

Treatment:

Drug: Ticagrelor

Drug: Prasugrel