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临床试验/NCT03228238
NCT03228238终止4 期

Effects of Long-term Vitamin C+E and Statin Therapy on Vasospasm Improvement and Regression of Atheroma in Patients With Variant Angina

Seoul National University Hospital2 个研究点 分布在 2 个国家目标入组 320 人开始时间: 2014年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
终止
入组人数
320
试验地点
2
主要终点
Vasospasm at 6 years

研究概览

简要总结

Purpose Objectives

  1. To evaluate the anti-oxidant effect of long-term Vitamin C+E therapy on coronary vasospasm improvement.
  2. To evaluate the anti-oxidant effect of long-term statin therapy on coronary vasospasm improvement.
  3. To evaluate the effect of long-term Vitamin C+E and statin therapy on regression of atheroma in target coronary vessels via intravascular ultrasound.
  4. To find out the role of vascular endothelium in variant angina via evaluating long-term Vitamin C+E and statin therapy on improvement in vascular endothelial function by assessing brachial arterial expansion capability.
  5. To find out the role of vascular endothelium in variant angina via evaluating long-term Vitamin C+E and statin therapy on improvement in arterial stiffness by assessing pulse wave velocity(PWV)

详细描述

Study Design: Prospective, open label, Four-arm, randomized single-center trial to test the effect long-term Vitamin C+E and Statin therapy on vasospasm improvement and regression of atheroma in patients with variant angina.

After provocation test, patients will be classified into three groups.(See below)

  1. Negative group : Patients who have symptoms that are consistent with vasospastic angina but only show luminal narrowing less than 50% on coronary angiography during provocation test.
  2. Mild Spastic group : Patients who have symptoms that are consistent with vasospastic angina and show luminal narrowing over 50% to less than 90% on coronary angiography during provocation test.
  3. Severe Spastic group : Patients who have symptoms that are consistent with vasospastic angina and show luminal narrowing over 90% on coronary angiography during provocation test.

In each group (except for patient in Negative group), patients will be randomized in a two by two factorial manner according to the study drug therapy (Vitamin C+E vs. no Vitamin C+E) (Statin vs. no Statin) As a result, patients in each group(except for patient in Negative group) will be randomized to 4 treatment subgroups, which are

  1. Control subgroup : Standard medication for Variant angina only
  2. Vitamin subgroup : Standard medication + Vitamin C+E
  3. Statin subgroup : Standard medication + Statin
  4. Dual subgroup : Standard medication + Vitamin C+E + Statin

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
None

入排标准

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

入选标准

  • Subject must be at least 30 years of age.
  • Subject is able to verbally confirm understandings of risks, benefits and treatment alternatives of receiving the Vitamin C+E or Statin or Dual, and he/she or his/her legally authorized representative provides written informed consent prior to any study related procedure.
  • Subject must have symptoms that are consistent with vasospastic angina with planned Coronary angiography and Provocation test.

排除标准

  • Patient who has organic coronary stenosis in main coronary branch at least 50% luminal narrowing after intracoronary nitroglycerin injection
  • Patient who has continuously taken Vitamin C or Vitamin E or Statin within 3months before Admission
  • Creatinine level ≥ 2.0mg/dL or dependence on dialysis.
  • Severe hepatic dysfunction (AST and ALT: 3 times upper normal reference values).
  • Active Myopathy or elevated Creatine kinase enzyme level (3 times upper normal reference values).
  • History of Severe hepatic dysfunction or Rhabdomyolysis due to statin side effect
  • Female of childbearing potential, unless a recent pregnancy test is negative, who possibly plan to become pregnant any time after enrollment into this study.
  • History of Urolithiasis
  • Non-cardiac co-morbid conditions are present with life expectancy <1 year or that may result in protocol non-compliance (per site investigator's medical judgment).

研究组 & 干预措施

Dual subgroup

Experimental

Standard medication for variant angina plus Vitamin C+E plus Statin Vitamin C and Vitamin E : Ascorbic acid Tablet 1g / Tocopherol Capsule 400IU Statin : Atorvastatin calcium 10mg

干预措施: Vitamin C and Vitamin E (Drug)

Statin subgroup

Experimental

Standard medication for variant angina plus Statin Statin : Atorvastatin calcium 10mg

干预措施: Statin (Drug)

Statin subgroup

Experimental

Standard medication for variant angina plus Statin Statin : Atorvastatin calcium 10mg

干预措施: Standard medication for variant angina (Drug)

Vitamin subgroup

Experimental

Standard medication for variant angina plus Vitamin C+E Vitamin C and Vitamin E : Ascorbic acid Tablet 1g / Tocopherol Capsule 400IU

干预措施: Vitamin C and Vitamin E (Drug)

Dual subgroup

Experimental

Standard medication for variant angina plus Vitamin C+E plus Statin Vitamin C and Vitamin E : Ascorbic acid Tablet 1g / Tocopherol Capsule 400IU Statin : Atorvastatin calcium 10mg

干预措施: Statin (Drug)

Vitamin subgroup

Experimental

Standard medication for variant angina plus Vitamin C+E Vitamin C and Vitamin E : Ascorbic acid Tablet 1g / Tocopherol Capsule 400IU

干预措施: Standard medication for variant angina (Drug)

Dual subgroup

Experimental

Standard medication for variant angina plus Vitamin C+E plus Statin Vitamin C and Vitamin E : Ascorbic acid Tablet 1g / Tocopherol Capsule 400IU Statin : Atorvastatin calcium 10mg

干预措施: Standard medication for variant angina (Drug)

Control group

Active Comparator

Control subgroup : Standard medication for Variant angina only

干预措施: Standard medication for variant angina (Drug)

结局指标

主要结局

Vasospasm at 6 years

时间窗: at 6 years

Severity of vasospasm in Vitamin subgroup, Statin subgroup, and Dual subgroup compared to control subgroup.

Vasospasm at 2 years

时间窗: at 2 years

Severity of vasospasm in Vitamin subgroup, Statin subgroup, and Dual subgroup compared to control subgroup.

Vasospasm at 6months

时间窗: at 6 months

Severity of vasospasm in Vitamin subgroup, Statin subgroup, and Dual subgroup compared to control subgroup.

Vasospasm at 4 years

时间窗: at 4 years

Severity of vasospasm in Vitamin subgroup, Statin subgroup, and Dual subgroup compared to control subgroup.

次要结局

  • Composed improvement of Arterial stiffness(Pulse wave velocity(PWV))(at 6 months, and at 2, 4, and 6 years follow up period)
  • Comparative analysis of improvement of Arterial stiffness(Pulse wave velocity(PWV))(at 6 months, and at 2, 4, and 6 years follow up period)
  • Improvement of Vascular endothelial function(Brachial arterial expansion capability)(at 6 months, and at 2, 4, and 6 years follow up period)
  • Composed improvement of Vascular endothelial function(Brachial arterial expansion capability)(at 6 months, and at 2, 4, and 6 years follow up period)
  • Changes from baseline in Vasospasm(at 6 months, and at 2, 4, and 6 years follow up period)
  • Comparative analysis of improvement of Vascular endothelial function(Brachial arterial expansion capability)(at 6 months, and at 2, 4, and 6 years follow up period)
  • Improvement of Arterial stiffness(Pulse wave velocity(PWV))(at 6 months, and at 2, 4, and 6 years follow up period)

研究者

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

Hyo-Soo Kim

Director of Cardiac Catheterization Laboratory & Coronary Intervention

Seoul National University Hospital

研究点 (2)

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