Status:
COMPLETED
Study of Cilostazol and Probucol Alone and in Combination on Atherosclerosis Related Biomarker---atherosclerosis Cerebral Infarction Patient as Study Subject
Lead Sponsor:
Otsuka Beijing Research Institute
Conditions:
Atherosclerosis Cerebral Infarction
Eligibility:
All Genders
40-80 years
Phase:
PHASE4
Brief Summary
Randomized, control, open label, multicentre clinical study. The patient who are in accordance with subject inclusion and exclusion criteria will be randomized to A group: Routine treatment B group: R...
Detailed Description
Efficacy index: After 12 weeks of treatment, the change difference of arteriosclerosis related biomarker between 4 modality groups. Pharmacokinetics: After 12 weeks of treatment, the study medicati...
Eligibility Criteria
Inclusion
- Inclusion Criteria:
- 40～80-year-old male or female
- By brain CT or MRI result, cerebral infarction is clarified diagnosis within 1 year
- With atherosclerosis, atherosclerosis should meet at least one of the conditions as below:
- Clarified diagnosis of type 2 diabetes before
- Clarified diagnosis of primary hypertension before
- Clarified diagnosis of Atherosclerotic stenosis in any 2 or more than 2 regions as cerebral artery, carotid, extremity artery and coronary by conformation of ultrasonic or angiography result
- Has Aspirin regularly for more than 1 month before registration
- Informed Consent Form signature
- Exclusion criteria：
- Has an allergic history to study drugs( including of Probucol and Cilostazol) and Aspirin
- Had lipid-lowing agents within the last 3 months ( except Statins)
- Had antiplatelet or anticoagulation agents within the last 3 months (except Aspirin)
- Had acute cerebral infarction within the last 1 month
- Has cardiogenic cerebral embolism
- At the registration ,Modified Rankin Scale ≥ 4
- Hemorrhagic tendency or hemorrhagic disease (such as cerebral hemorrhage, gastrointestinal tract hemorrhage, etc.)
- Had a myocardial infarction, angina pectoris within the last 3 months
- Congestive heart failure
- Is pregnant, is potentially pregnant, or is breastfeeding
- Severe hepatic inadequacy or severe renal inadequacy (AST or ALT is 2.5 times higher than the upper limit of the normal value range, or serum creatinine is 1.2 times higher than the upper limit of the normal value range)
- Persistent or hardly controlled hypertension (such as malignant hypertension, BP\> 160/100 mmHg)
- Severe ventricular arrhythmia (such as multiple and multifocal premature ventricular contractions)
- Has a medical history that includes a cardiac syncope or a primary syncope
- Has a condition that may prolong QT interval (such as congenital long QT syndrome, taking drugs which prolong QT interval, hypokalemia or hypomagnesemia, etc.)
- Has severe diseases (such as, malignant tumor, severe anaemia, severe hematologic diabetes mellitus ketoacidosis, nonketotic hyperosmolar diabetic coma, etc.)
- Registered other clinical trails within the last 3 months
- Has vasculitis, moyamoya disease and other non-atherosclerosis vascular diseases
- Other conditions that could exclude the subject from this study by doctor's judgment
Exclusion
Key Trial Info
Start Date :
March 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
July 1 2010
Estimated Enrollment :
200 Patients enrolled
Trial Details
Trial ID
NCT00823875
Start Date
March 1 2009
End Date
July 1 2010
Last Update
December 1 2010
Active Locations (1)
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1
First Affliate Hospital of Beijing University
Beijing, China