Comparison of Vascular Remodeling Between Different Antianginal Medication Evaluated by Noninvasive ECG-gated Fundus Photographic Evaluation
NCT ID: NCT01162902
Last Updated: 2013-12-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE4
150 participants
INTERVENTIONAL
2013-09-30
2015-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Diltiazem treated group
Diltiazem 180mg treated group
Diltiazem treated group
Diltiazem 180mg for 9 months
Bisoprolol treated group
Bisoprolol 5mg treated group
Bisoprolol treated group
Bisoprolol 5mg for 9 months
Candesartan treated group
Candesartan 32mg treated group
Candesartan treated group
Candesartan 32mg for 9 months
Interventions
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Diltiazem treated group
Diltiazem 180mg for 9 months
Bisoprolol treated group
Bisoprolol 5mg for 9 months
Candesartan treated group
Candesartan 32mg for 9 months
Eligibility Criteria
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Inclusion Criteria
* Unstable Angina/NSTEMI patients who completed PCI for main lesions
* Either systolic \> 130mmHg or diastolic \> 80mmHg, or patients with anti-hypertensive drugs
Exclusion Criteria
* Variant Angina
* Liver function abnormality or renal failure
* History of Hypersensitivity to testing drugs
* Severe heart failure(NYHA class\>3) or uncorrectable hematologic disease
* Woman possible to be pregnant
* Uncontrolled diabetes
* Expected life span \< one year
30 Years
80 Years
ALL
No
Sponsors
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Seoul National University Hospital
OTHER
Responsible Party
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Seoul National University Hospital
Locations
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Seoul National University Hospital
Seoul, , South Korea
Countries
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Central Contacts
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Other Identifiers
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ABC Trial
Identifier Type: -
Identifier Source: org_study_id
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