Endothelium, Stenting, and Antiplatelet Therapy (EST) - Clopidogrel, Prasugrel, Ticagrelor Study (EST)
2016年9月4日 更新者:Tommaso Gori、Johannes Gutenberg University Mainz
Effects of Clopidogrel vs Prasugel vs Ticagrelor on Endothelial Function, Inflammatory and Oxidative Stress Parameters and Platelet Function in Patients Undergoing Coronary Artery Stenting. A Randomised, Prospective Study.
Endothelial dysfunction is an important predictor - and a determinant - of adverse clinical outcome.
Endothelial function is impaired by coronary artery stenting, a stud from our group has shown that it can be improved by platelet inhibition using clopidogrel.
However, clopidogrel unresponsiveness is a known problem, and it has been show that the endothelial effects of clopidogrel tend to wane upon prolonged treatment.
Whether a more effective anti-platelet therapy is able to prevent/improve not only thrombotic events but also endothelial dysfunction, with potential positive impact on clinical outcome in patients undergoing coronary artery stenting, is an important hypothesis that needs to be further investigated.
To date, evidence regarding "ancillary" (non-platelet-dependent) effects of antiaggregant drugs is very limited.
For instance, while their antiplatelet effects, and their beneficial effects in patients with acute coronary syndromes, have been clearly demonstrated in multicentric trials, it remains to be shown whether these drugs also protect endothelial function.
Interestingly, some authors suggest that the mortality benefit observed in the PLATO study is at least in part independent of direct antiplatelet effects.
No study, to date, has tested the effects of prasugrel and/or ticagrelor on endothelial function.
With the present trial, the investigators plan to test the effect of clopidogrel, prasugrel and ticagrelor on endothelial function before and up to 4 weeks after coronary artery stenting.
This study will provide important pathophysiologic insight on the relationship between platelet aggregation and endothelial function, two parameters that have been shown to influence patients' prognosis.
研究概览
研究类型
介入性
注册 (实际的)
126
阶段
- 第四阶段
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
-
Mainz、德国、55131
- 2 Medical Clinic
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 75年 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
- - 18-75 years old consecutive patients undergoing coronary angiography and stenting at the University Medical Centre Mainz
- A coronary lesion (and patient) amenable to treatment with drug eluting stent
- Ability of subject to understand character and individual consequences of clinical trial
- Signed and dated informed consent of the subject must be available before start of any specific trial procedures.
- Negative pregnancy test of women with childbearing potential
Exclusion Criteria:
- Subjects presenting 1 or more of the following criteria will not be enrolled in the trial:
- Patients with elevated (> 5 times upper normal limit) C-reactive protein level prior to stenting
- Patients in whom therapy with long-acting nitrates cannot be suspended prior to endothelial function measurements
- An acute coronary syndrome treated with coronary stenting within the last 4 weeks
- Patients with known inflammatory/infective diseases
- Patients with severe extracardiac diseases limiting life expectancy
- Known heart failure (LV-EF ≤ 40% AND NYHA III-IV)
- PCI or coronary By-Pass surgery within the last 4 weeks, pre-existing ongoing treatment with any of the study treatments.
- History of cerebrovascular events (stroke)
- Known renal dysfunction (serum creatinine ≥ 1.8mg/dl in women, ≥ 2.0mg/dl in men)
- Serum potassium > 5.5mmol/l
- Known hepatic impairment (AST, ALT > 3 times upper limit of normal)
- Changes in the ß-blocker, statin or ACE or angiotensin-receptor blocker inhibitor treatment within the past 2 weeks
- Pregnancy and lactation, inadequate contraception
- Body weight < 60kg
- Active bleeding
- Therapy with CYP3A4 inhibitors (ketoconazole, protease inhibitors, macrolide antibiotics)
- Therapy with anticoagulants: phenprocoumone, warfarin, dabigatran, rivaroxaban
- History of hypersensitivity to any of the investigational medicinal products or to any drug with similar chemical structure or to any excipient present in the pharmaceutical form of the investigational medicinal product.
- Ongoing participation in other clinical trials or within the last 3 months, or ongoing therapy with one of the study medications.
- Medical or psychological condition that would not permit completion of the trial or signing of informed consent.
- Patients with acute ST-elevation myocardial infarction
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:基础科学
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
有源比较器:Ticagrelor
Ticagrelor 180mg oral loading dose and 90mg b.i.d for 30 days following coronary artery stenting
|
All patients will receive a drug eluting stent as clinically indicated.
Ticagrelor 180mg oral loading dose and 90mg b.i.d for 30 days following coronary artery stenting
|
|
有源比较器:Clopidogrel
Clopidogrel 600mg loading dose + 75 mg once a day for 30 days following coronary artery stenting.
|
All patients will receive a drug eluting stent as clinically indicated.
Clopidogrel 600mg loading dose + 75 mg once a day for 30 days following coronary artery stenting.
|
|
有源比较器:Prasugrel
Prasugrel 60mg oral loading dose followed by 10mg once a day for 30 days following coronary artery stenting
|
All patients will receive a drug eluting stent as clinically indicated.
Prasugrel 60mg oral loading dose followed by 10mg once a day for 30 days following coronary artery stenting
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Change in FMD
大体时间:baseline and 1 month
|
The primary endpoint is the change in flow-mediated dilation (FMD) (comparison before treatment versus after treatment and stenting) in the three study groups.
The mean FMD across the three measurements (1 day, 1 week, 1 month) performed after coronary artery stenting will be compared to the FMD value before drug administration and stenting.
|
baseline and 1 month
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
FMD 2 hours after loading dose
大体时间:baseline and 2 hours after loading dose
|
Change in FMD 2 hours after the administration of the study drug
|
baseline and 2 hours after loading dose
|
|
L-FMC at 2 hours after the loading dose
大体时间:baseline and 2 hours
|
change in L-FMC at two hours after the loading dose
|
baseline and 2 hours
|
|
L-FMC 1 month after loading dose
大体时间:baseline and 1 day after stenting
|
change in flow-mediated constriction (L-FMC) (comparison before treatment versus after treatment and stenting) in the three study groups.
The mean L-FMC across the three measurements (1 day, 1 week, 1 month) performed after coronary artery stenting will be compared to the value before drug administration and stenting
|
baseline and 1 day after stenting
|
|
Safety and tolerability
大体时间:from baseline to 1 month after enrollment
|
Number of patients with adverse events.
|
from baseline to 1 month after enrollment
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 学习椅:Thomas Munzel, MD Prof.、University Medical Center Mainz
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
一般刊物
- Schnorbus B, Jurk K, Lackner KJ, Welk C, Munzel T, Gori T. Effects of Clopidogrel, Prasugrel and Ticagrelor on Microvascular Function and Platelet Reactivity in Patients With Acute Coronary Syndrome Undergoing Coronary Artery Stenting. A Randomized, Blinded, Parallel Group Trial. Front Cardiovasc Med. 2021 Dec 13;8:780605. doi: 10.3389/fcvm.2021.780605. eCollection 2021.
- Schnorbus B, Daiber A, Jurk K, Warnke S, Konig J, Krahn U, Lackner K, Munzel T, Gori T. Effects of clopidogrel, prasugrel and ticagrelor on endothelial function, inflammatory and oxidative stress parameters and platelet function in patients undergoing coronary artery stenting for an acute coronary syndrome. A randomised, prospective, controlled study. BMJ Open. 2014 May 6;4(5):e005268. doi: 10.1136/bmjopen-2014-005268.
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2012年8月1日
初级完成 (实际的)
2016年7月1日
研究完成 (实际的)
2016年9月1日
研究注册日期
首次提交
2012年9月4日
首先提交符合 QC 标准的
2012年10月3日
首次发布 (估计)
2012年10月4日
研究记录更新
最后更新发布 (估计)
2016年9月7日
上次提交的符合 QC 标准的更新
2016年9月4日
最后验证
2016年9月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.