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临床试验/NCT02108808
NCT02108808已完成4 期

Differential Effect of Ticagrelor vs Prasugrel or Clopidogrel Loading on Fractional Flow Reserve

University of Patras1 个研究点 分布在 1 个国家目标入组 76 人开始时间: 2014年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
76
试验地点
1
主要终点
% relative change in steady hyperemia FFR (sFFR)

研究概览

简要总结

Fractional flow reserve (FFR) is an established invasive method for assessing the physiological significance of coronary artery stenosis. Adenosine, an important endogenous regulator of coronary blood flow during both stress and ischemia, is widely used to achieve conditions of stable hyperemia required for measurement of FFR.

Studies in healthy volunteers and in patients with acute coronary syndrome (ACS) post percutaneous coronary intervention (PCI) receiving ticagrelor revealed a differential coronary blood flow velocity response during increasing doses of adenosine compared to placebo or prasugrel treated subjects, respectively. It has also been demonstrated that patients treated with ticagrelor have increased plasma adenosine levels. Therefore, it has been hypothesized that the degree of hyperemia obtained with adenosine infusion may be greater in patients on ticagrelor than that obtained in patients taking clopidogrel or prasugrel. If this proves to be true, it would lead to a lower FFR value with possible important clinical implications in ticagrelor receiving patients in need for FFR measurement.

This is a prospective, single center, randomized study of parallel design. Consecutive ticagrelor naive patients who are referred for coronary angiography and have an angiographically moderate to severe de novo stenosis (>50% and <90% diameter by visual assessment) in at least one major epicardial coronary artery amenable to PCI are candidates for this study. Patients after informed consent will be randomized (hour 0) to receive immediately post FFR (with adenosine iintravenous infusion at 140 μg/Kg/min for a 3 minute period) either ticagrelor 180mg loading dose or prasugrel 60mg/clopidogrel 600mg loading dose (as clinically indicated). FFR examination will be repeated 2 hours post loading dose.

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 (Investigator)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-80 years
  • Patients subjected to clinically indicated coronary angiography with at least one 50%-90% stenosis at 1 major epicardial vessel (by visual assessment) amenable to percutaneous coronary intervention.
  • Ticagrelor naive patients
  • Written informed consent

排除标准

  • History of coronary artery bypass surgery
  • Acute myocardial infarction within the previous 5 days
  • Known allergy to adenosine, ticagrelor, prasugrel or clopidogrel
  • Prior intracranial hemorrhage
  • Hemodialysis or creatinine clearance < 30ml/h
  • Moderate/severe hepatic failure
  • Active bleeding, or at increased risk of bleeding
  • Left ventricular ejection fraction <40%
  • Primary myocardial or valvular disease
  • Contraindication to adenosine
  • Angiographically visible thrombus at a target lesion, extremely tortuous coronary arteries, severely calcified lesions, left main disease, anatomy suitable for coronary artery bypass surgery
  • Previous q wave myocardial infarction in the area of target vessel
  • Severe left ventricular hypertrophy
  • Severe valvular heart disease
  • Heart failure as defined by New York Heart Association class III or IV 16.Hypotension (blood pressure <90 mm Hg)
  • 17.Significant arrhythmia (e.g. excessive premature ventricular contractions or atrial fibrillation), tachycardia (heart rate >120 beats/min), bradycardia (<50 beats/min), increased risk for bradycardia 18.Caffeine consumption or cigarette smoking within the previous 24 hours.

研究组 & 干预措施

Ticagrelor

Experimental

Ticagrelor 180mg loading dose

干预措施: Ticagrelor (Drug)

Prasugrel or Clopidogrel

Active Comparator

Prasugrel 60mg or Clopidogrel 600mg loading dose, as clinically indicated

干预措施: Prasugrel or Clopidogrel (Drug)

结局指标

主要结局

% relative change in steady hyperemia FFR (sFFR)

时间窗: 2 hours

Steady hyperemia FFR (sFFR) is defined as the FFR value attained during stable hyperemia (as assessed by offline visual inspection of the 3-min hemodynamic trace) (sFFR post drug - sFFR pre drug)\*100/sFFR pre drug between the 2 treatment arms

次要结局

  • % relative change in lowest FFR (lFFR)(2 hours)
  • % relative change in peak hyperemia FFR (pFFR)(2 hours)
  • % relative change in time to peak FFR (in seconds)(2 hours)
  • % relative change in time to lowest FFR(2 hours)
  • % relative change in area under the curve (AUC) of the FFR trace(2 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dimitrios Alexopoulos

Professor of Cardiology

University of Patras

研究点 (1)

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