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临床试验/NCT02325466
NCT02325466已完成3 期

Comparative Efficacy of Ticagrelor Versus Aspirin on Blood Viscosity in Peripheral Artery Disease (PAD) Patients With Type 2 Diabetes (T2D)

Icahn School of Medicine at Mount Sinai1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2015年4月最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
入组人数
70
试验地点
1
主要终点
Mean Change in Low Shear Blood Viscosity

研究概览

简要总结

The hypothesis being that both aspirin-ticagrelor and ticagrelor monotherapy will be superior to aspirin monotherapy in the reduction of whole blood viscosity at the end of each 4 week treatment period. Study participants will be randomized into 3 groups, and each group will receive each of 3 treatments in the cross-over study. At the end of each individual 4 week treatment period the investigators will determine whether there are differences in low and high shear rate dependent viscosity and investigate the effect of the treatment on peripheral arterial blood flow using pulse volume recordings, ankle brachial index and toe pressures. Subjects will be eligible if they have ankle-brachial index less than or equal to 0.85, or if a patient's blood vessels are calcified, patients will have toe-brachial index less than or equal to 0.6 performed using continuous-wave Doppler.

详细描述

Ticagrelor has been shown to significantly reduce the rate of cardiovascular disease (CVD) events and death compared with clopidogrel in patients having prior acute coronary syndrome. A number of outcome studies have demonstrated the risk of major CVD events increased with blood viscosity. Stroke patients and those with stroke risk factors were shown to have chronically elevated blood viscosity relative to healthy controls. Based on prior observations, the rationale for this study is to demonstrate that both aspirin-ticagrelor and ticagrelor monotherapy will be superior to aspirin monotherapy in the reduction of whole blood viscosity at the end of each 4 week treatment period.

The primary objectives for this study is to: (1) Compare the effect of aspirin-ticagrelor with aspirin in a double blind, randomized, cross-over study design (weeks 1-4, weeks 6-10, and weeks 12-16) on blood viscosity at both low (5 s-¹) and high (300 s-¹) shear rates at the end of each 4-week treatment period; and (2) to compare the effect of ticagrelor mono-therapy with aspirin in a double blind, randomized, cross-over study design (weeks 1-4, weeks 6-10, and weeks 12-16) on blood viscosity at both low (5 s-¹) and high (300 s-¹) at the end of each 4-week treatment.

The secondary objectives for this study include: (1) a determination as to whether there are differences in low and high shear rate dependent viscosity with treatment by ticagrelor alone and combination aspirin-ticagrelor. Additionally, investigated will be the effect of the treatment on peripheral arterial blood flow using pulse volume recordings, ankle brachial index, and toe pressures.

The general approach to evaluation of drug efficacy will be through blood samples collected with a standard venipuncture for viscosity testing. Blood viscosity will be measured using an automated scanning capillary tube viscometer across a physiologic range of shear rates of 1-1000 s-1 in increments of 0.1 s-1. Blood viscosity levels at 5 s-1 will be reported as low-shear viscosity, and blood viscosity measurements at 300 s-1 will be reported as high-shear viscosity. Additionally, pulse volume recordings will be simultaneously obtained at the level of the ankle, metatarsal and toe bilaterally according to standard protocol, and Continuous-wave Doppler will be used to determine ankle-brachial indices or toe-brachial indices, and flow velocity profiles.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

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

入选标准

  • Female or male aged ≥ 35 years
  • Type 2 diabetes mellitus
  • Symptomatic PAD
  • Ankle-brachial index ≤ 0.85 or calcified blood vessels with toe-brachial index ≤ 0.6 and/or abnormal post-exercise ankle-brachial index
  • Prior surgical or percutaneous intervention of the peripheral arteries ≥12 months previously with a residual stenoses of ≥50% in a non-dilated artery.

排除标准

  • Subject is pregnant or breast-feeding
  • Planned revascularization or amputation
  • Known bleeding disorder
  • History of intracranial hemorrhag3
  • Considered at risk of hemorrhagic events
  • Hypersensitivity or allergic reactions to aspirin
  • Concomitant use of anticoagulants such as warfarin, dabigatran, factor Xa inhibitors or antiplatelet drugs such as clopidogrel, dipyridamole and sulfapyridine
  • Subject has a condition or circumstance which would prevent them from adhering to treatment regimens
  • Subject has active infection
  • Subject has an anemia
  • Subject has given blood or received a blood transfusion at any point during the study
  • Subject has polycythemia vera or any hyperviscosity syndrome
  • Subjects with Waldenstrom's macroglobulinemia who have an increased risk of hyperviscosity syndrome
  • Subject has history of severe liver disease, obstructive liver disease such as primary biliary cirrhosis or end-stage renal disease (eGFR <30 mL/min/m2)
  • Family members or employees of the investigator or study centers involved in the study
  • Subject has poor diabetes or hypertension control (systolic blood pressure ≥ 180 mmHg or diastolic blood pressure ≥ 100 mmHg)

研究组 & 干预措施

Aspirin/Ticagrelor placebo

Placebo Comparator

aspirin 81 mg daily and ticagrelor placebo twice daily

干预措施: Aspirin (Drug)

Aspirin/Ticagrelor placebo

Placebo Comparator

aspirin 81 mg daily and ticagrelor placebo twice daily

干预措施: Ticagrelor Placebo (Drug)

Aspirin/Ticagrelor

Active Comparator

aspirin 81 mg daily and ticagrelor 90 mg twice daily

干预措施: Aspirin (Drug)

Aspirin/Ticagrelor

Active Comparator

aspirin 81 mg daily and ticagrelor 90 mg twice daily

干预措施: Ticagrelor (Drug)

Aspirin Placebo/Ticagrelor

Active Comparator

aspirin placebo daily and ticagrelor 90 mg twice daily

干预措施: Ticagrelor (Drug)

Aspirin Placebo/Ticagrelor

Active Comparator

aspirin placebo daily and ticagrelor 90 mg twice daily

干预措施: Aspirin Placebo (Drug)

结局指标

主要结局

Mean Change in Low Shear Blood Viscosity

时间窗: baseline, week 16

Compare the effect of aspirin-ticagrelor and ticagrelor monotherapy with aspirin on blood viscosity from week 16 to baseline

Mean Change in High Shear Blood Viscosity

时间窗: baseline and week 16

Compare the effect of aspirin-ticagrelor and ticagrelor monotherapy with aspirin on blood viscosity at week 16 to baseline

次要结局

  • Mean Change in Peripheral Arterial Blood Flow(baseline and week 16)
  • Mean Change in Microvascular Blood Flow Composite Score(baseline and week 16)

研究者

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

Robert Rosenson

Professor Medicine, Cardiology

Icahn School of Medicine at Mount Sinai

研究点 (1)

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