EUCTR2014-000197-19-IT进行中(未招募)1 期
Assessment of Coronary Flow Reserve by Doppler Flow WIre in Patients With Acute Coronary Syndrome Undergoing PercuTaneous Coronary Intervention: DiffErences Between the LoAding Dose of Ticagrelor and PrasugrEl. - DELATE
MBERTO I - POLICLINICO DI ROMA0 个研究点目标入组 90 人开始时间: 2021年10月1日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 90
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Patients with ACS (acute coronary syndromes) undergoing PCI with
- •stent implantation;
- •Patients = 18 and = 75 years old;
- •Signed informed consent.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 20
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 70
排除标准
- •Patients with stable angina;
- •prior myocardial infarction;
- •prior revascularization (PCI or CABG-coronary artery bypass
- •Prasugrel and/or Ticagrelor contraindications (history of intracranial
- •hemorrhage, active pathological bleeding, severe hepatic impairment);
- •major periprocedural complications;
- •GFR ( glomerular filtration rate) < 30 ml/min or requiring
- •haemodialysis;
- •Non-sinus rhythm;
- •severe COPD (chronic obstructive pulmonary disease);
- •requirement for oral anticoagulant;
- •risk of bleeding or bradycardic events;
- •EF (ejection fraction) < 45%;
- •Cardiogenic shock;
- •Severe left ventricular hypertrophy;
- •severe valvular disease;
- •indication to CABG;
- •diffuse coronary atherosclerosis;
研究者
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