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
35000 participants
OBSERVATIONAL
2009-01-31
2017-10-31
Brief Summary
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Detailed Description
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All potential patients will be screened for the eligibility in a screening visit. Those who fill the inclusion criteria at screening will be invited for the registry study into different groups. The follow-up will take place yearly thereafter for 5 years, through clinical visiting, phone follow-up, or records from the NHIB Taiwan. At each clinical visit, vital signs, clinical endpoints, adverse events, concurrent medication information and laboratory specimens will be obtained as complete as possible. With phone or records from NHIB, only clinical endpoints will be recorded. If the primary care physician intends to treat the patient's lipid profile to the target, he/she can add, delete or adjust the LLT by his/her clinical judgement.
Conditions
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Keywords
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Study Design
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CASE_ONLY
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* One without ASVD but with at least 1 CV risk factor
* Apparent healthy persons
Exclusion Criteria
* One with any non-cardiovascular diseases which may affect prognosis
20 Years
90 Years
ALL
Yes
Sponsors
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National Taiwan University Hospital
OTHER
Responsible Party
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Principal Investigators
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Locations
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NTUH
Taipei, , Taiwan
Countries
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Central Contacts
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Facility Contacts
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C C W
Role: primary
Other Identifiers
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200910021R
Identifier Type: -
Identifier Source: org_study_id