To Evaluate the Efficacy and Safety of Cilostazol in subject with VSA
- Conditions
- Diseases of the circulatory system
- Registration Number
- KCT0001561
- Lead Sponsor
- Korea Otsuka Pharmaceuticals
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
1) Male or female 20 or over the age of 20 and under the age of 80.
2) Patients showing angina attack even while resting during the screening, diagnosed with vasospastic angina within the previous 3 months by meeting at least one of the 3 definitions, and accompanying insignificant (stenosis rate <50%) coronary artery disease documented by coronary angiography within the last 3 months [temporary antispastic agents (monotherapies or a combination of Verapamil and Nitroglycerin, anticoagulants) for coronary angiography are allowed]
- Chest pain accompanied by at least 2 temporary, closely located ST elevations or depressions of 0.1mV or greater in the absence of ergonovine provoked coronary angiography
- Positive Intracoronary (IC) or Intravenous (IV) Ergonovine provocation test; ischemic ECG change accompanied by chest pain and spasm reducing the coronary diameter by 90% or more (at least 2 temporary, closely located ST elevations or depressions of 0.1mV or greater on 12-lead ECG)
3) Patients who reported at least 1 episode of chest pain in a week during amlodipine run-in period and at least 2 episodes in the final week
4) Women who had been menopausal or sterile for at least 1 year, or women of childbearing potential who agree to practice a contraceptive measure throughout the clinical trial (e.g., hormonal contraceptives, intrauterine devices, condom + spermicidal agents, diaphragm + spermicidal agents, and partner’s infertility)
5) Subjects who signed a written agreement indicating that they were given full explanations of the clinical trial and are willing to participate in the clinical trial
1) Subjects who used Cilostazol within 3 months before the screening visit
2) Subjects who used antiplatelet drugs, including Aspirin, Clopidogrel, Ticlopidine and Sarpogrelate, or PDE3 inhibitors of the same class as Cilostazol, such as Amrinone, Milrinone and Enoximone, after the initiation of the amlodipine run-in period
3) Subjects who used oral anticoagulants, such as warfarin, within 1 months prior to the screening visit
4)Subjects who used any of the following drugs within 1 week prior to the screening visit
- CCBs apart from amlodipine
- Beta-blockers or alpha-blockers
- Oral nitrate, excluding nitroglycerin sublingual tablet, Nicorandil
- Vitamin E preparations
- Estrogens
5) History of myocardial infarction or with myocardial infarction mediated by vasospastic angina at the time of screening
6) History of a life-threatening vasospastic event (e.g., ventricular tachycardia, atrial fibrillation or syncope)
7) History of stroke, intracranial hemorrhage or transient ischemic attack (TIA)
8) Hemorrhage (hemophilia, capillary fragility, upper gastrointestinal bleeding, urinary tract bleeding, hemoptysis, vitreous hemorrhage, etc.) or such predisposition (active peptic ulcer, hemorrhage suspected at Cilostazol administration for surgical wound within the last 3 months, proliferative diabetic retinopathy)
9) History of hypersensitivity to the ingredients of Cilostazol, amlodipine, dihydropyridines such as nitroglycerine, and nitrates
10) Severe aortic stenosis
11) History of shock
12) Hypotension with systolic pressure of below 90mmHg at screening
13) Severe anemia with hemoglobin 6.5g/dl or below at screening
14) History of glaucoma
15) ST change abnormality not interpretable on ECG at screening
16) Congestive heart failure with left ventricular ejection fraction <40% on echocardiography at screening or within the last 3 months
17) Atrial fibrillation or beyond moderate valvular heart disease
18) Left main coronary spasm suspected or confirmed by coronary angiography or ergonovine provoked coronary angiography
19) History of coronary artery bypass graft (CABG) or percutaneous coronary intervention (PCI)
20) Heart rate >100 bpm at screening via vital sign: tachycardia
21) Uncontrolled hypertension with systolic pressure = 160 mmHg or diastolic pressure = 100 mmHg at screening
22) Creatinine level = 1.5 mg/dL at screening
23) AST or ALT > x3 ULN(Upper Limit of Normal) at screening
24) Platelet count < 100,000mm3 at screening
25) QT prolongation of QTcB > 450 msec in male and QTcB> 470 msec in female subjects at screening
26) Women of childbearing potential with positive pregnancy test at screening
27) Women who did not agree to practice a contraceptive measure, pregnant or lactating women
28) Drug compliance of less than 80% during 2-week amlodipine run-in period
29) Subjects otherwise judged by the investigator to be inappropriate for inclusion in the trial
30) Subjects who used another investigational products within 2 months prior to the randomization
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in the frequency of chest pain between the week before and the final week of investigational products administration
- Secondary Outcome Measures
Name Time Method Percent change in the frequency of chest pain between the week before and the final week of investigational products administration;Proportion of the subjects whose chest pain was not present in the final week of investigational products administration;Change in pain intensity between the week before and the final week of investigational products administration;Mean change in pain intensity (overall pain intensity/frequency of pain) between the week before and the final week of investigational products administration;Change in total dose of nitroglycerin sublingual tablets used between the week before and the final week of investigational products administration