Facilitation Through Aggrastat or Cangrelor Bolus and Infusion Over prasugreL: a mUlticenter Randomized Open-label Trial in patientS With ST-elevation Myocardial inFarction Referred for primAry percutaneouS inTERvention.FABOLUS FASTER Trial
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 122
- 试验地点
- 3
- 主要终点
- Inhibition of platelet activity (IPA, %) with LTA-ADP 20 µmol/l
研究概览
简要总结
Primary percutaneous coronary intervention (PCI) is the main reperfusion therapy in patients with ST-elevation myocardial infarction (STEMI). The optimal platelet inhibition at the time of PCI is fundamental, however, the comparative speed of action of cangrelor as opposed to tirofiban and to chewed or integer loading dose of prasugrel is unknown.
The purpose of this trial is to assess the inhibition of platelet aggregation with different regimens on platelet inhibition (tirofiban bolus+infusion, cangrelor bolus+infusion, prasugrel chewed loading dose, prasugrel integer loading dose) in the early phase of primary PCI.
详细描述
Primary percutaneous coronary intervention (PCI) is the main reperfusion therapy in patients with ST-elevation myocardial infarction (STEMI). Ancillary pharmacological therapy includes dual antiplatelet therapy with aspirin and an inhibitor of P2Y12 receptor, responsible of adenosine diphosphate(ADP)-mediated platelet activation.Prasugrel and ticagrelor are the most recent and efficient oral P2Y12 inhibitors available to date. However, in STEMI even prasugrel and ticagrelor could have a significant delay of onset of action. Early in-ambulance administration can increase the inhibition of P2Y12 receptor, however, the benefits versus risks balance remain uncertain. Recently, small-scale independent studies suggested that chewed or crushed loading dose of ticagrelor or prasugrel can achieve more pronounced platelet inhibition compared with standard whole tablets soon after drug administration. Yet, the delay in platelet inhibition remains considerable even after chewed or crushed loading dose of newer oral P2Y12 inhibitors and suboptimal modulation of platelet reactivity at the time of primary intervention may persist. Tirofiban and cangrelor are intravenous drugs with a more rapid onset and offset of action compared with oral agents. Both agents have been extensively tested in clinical trials including patients with STEMI. However, the comparative speed of action of cangrelor as opposed to tirofiban and to chewed or integer loading dose of prasugrel is unknown. The proposed investigation will have a prospective, randomized, design in which STEMI patients undergoing primary PCI will be randomized to receive Cangrelor or Tirofiban or Prasugrel (these patients will be further randomized to receive chewed or integer tablets). Pharmacodynamic testing will be performed at several time points to test the investigators' study hypotheses: 1) Cangrelor will have similar inhibitory effect to Tirofiban (non-inferiority of Cangrelor compared with Tirofiban); 2) Compared with Prasugrel, Cangrelor and Tirofiban will achieve more prompt and enhanced platelet inhibitory effects (superiority of both Tirofiban and Cangrelor to integer Prasugrel); 3) Compared with integer loading dose of Prasugrel, chewed Prasugrel regimen will achieve more prompt and enhanced platelet inhibitory effects (superiority of chewed Prasugrel to integer Prasugrel). This study will provide insights on the pharmacodynamic effects of these drugs and will help clinicians choose the most appropriate treatment to avoid complications related to inadequate platelet inhibition in the early phase of patients with STEMI undergoing primary PCI.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
盲法说明
The study is open label. Participant and Investigators will be not masked to randomly assigned treatments. An independent blinded committee will assess clinical adverse events.
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age greater than 18 years old
- •ST-segment elevation myocardial infarction
- •Referred for primary PCI either within 12 h of symptom onset or between 12 and 24 h after onset with evidence of continuing ischemia
排除标准
- •Unconsciousness
- •Other conditions that make the patient incapable receiving integer loading dose of prasugrel
- •Any contraindication and/or known hypersensitivity or allergy to aspirin, prasugrel, intravenous unfractionated heparin, cangrelor, tirofiban
- •Any contraindication to primary PCI
- •Administration of glycoprotein IIb/IIIa inhibitors (GPI) or P2Y12-inhibitors or cangrelor < 7 days
- •Chronic dialysis
- •Recent (< 15 days) or current major bleeding
- •Recent (< 15 days) major surgery
- •Administration of fibrinolytics < 30 days
- •Current use or indication to oral anticoagulant
- •Previous stroke or transient ischemic attack (TIA)
- •Inability to follow the procedures of the study (language problems, psychological disorders, dementia) or comorbidities associated with less than 6 months survival (active malignancies drug or alcohol abuse, etc.)
- •Women who are pregnant or breast feeding or with potential to become pregnant during the course of the study (age < 55 years and last menstruation within the last 12 months) and did not undergo tubal ligation, ovariectomy or hysterectomy
- •Participation in another study with investigational drug within the 30 days preceding and during the present study
- •Enrolment of the investigator, his/her family members, employees and other dependent persons
研究组 & 干预措施
Cangrelor
Cangrelor bolus of 30 µg/Kg followed by infusion at 4 µg/Kg/min for 2 h (or to the end of PCI).
干预措施: Cangrelor (Drug)
Tirofiban
Tirofiban bolus of 25 µg/Kg bolus followed by infusion at 0.15 µg/Kg/min for 2 h (or to the end of PCI) (infusion rate of 0.075 µg/Kg/min for patients with creatinine clearance < 60 ml/min).
干预措施: Tirofiban (Drug)
Prasugrel
Prasugrel oral integer or chewed at an identical loading dose of 60 mg
干预措施: Prasugrel (Drug)
结局指标
主要结局
Inhibition of platelet activity (IPA, %) with LTA-ADP 20 µmol/l
时间窗: 30 minutes
Primary outcome is platelet inhibition assessed with light transmission aggregometry (LTA) in platelet rich plasma with the addition of adenosine diphosphate (ADP) 20 µmol/l at 30 minutes from drug administration
次要结局
- Inhibition of platelet activity (IPA, %) with LTA-ADP 5 µmol/l(15 minutes, 30 minutes, 1 hour, 2 hours, 3 hours, 4-6 hours)
- Inhibition of platelet activity (IPA, %) with LTA-TRAP 5 µmol/l(15 minutes, 30 minutes, 1 hour, 2 hours, 3 hours, 4-6 hours)
- Inhibition of platelet activity (IPA, %) with LTA-TRAP 15 µmol/l(15 minutes, 30 minutes, 1 hour, 2 hours, 3 hours, 4-6 hours)
- Area under the curve (AUC) at Multiplate with ADP test(15 minutes, 30 minutes, 1 hour, 2 hours, 3 hours, 4-6 hours)
- Area under the curve (AUC) at Multiplate with TRAP test(15 minutes, 30 minutes, 1 hour, 2 hours, 3 hours, 4-6 hours)
- Angiographic result(immediately after PCI procedure)
- Intramyocardial haemorrhage at Cardiac Magnetic Resonance Imaging (MRI)(3 days and 4-6 months after PCI)
- Major adverse ischemic clinical events(48 h and 30 days after PCI)
- Bleeding events(48 h and 30 days after PCI)
- Electrocardiographic result(immediately after PCI procedure and 90 minutes after PCI)
- Inhibition of platelet activity (IPA, %) with LTA-ADP 20 µmol/l(15 minutes, 1 hour, 2 hours, 3 hours, 4-6 hours)
- Infarct size at Cardiac Magnetic Resonance Imaging (MRI)(3 days and 4-6 months after PCI)