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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TERMINATED
67 participants
OBSERVATIONAL
2017-08-01
2018-04-03
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Normouricemia
Serum uric of 7mg/dl or less in men or 6mg/dl or less in women
hyperuricemia
serum uric acid of 7mg/dl or more in men or 6mg/dl or more in women
Hyperuricemia
Serum uric of 7mg/dl or more in men or 6mg/dl or more in women
hyperuricemia
serum uric acid of 7mg/dl or more in men or 6mg/dl or more in women
Interventions
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hyperuricemia
serum uric acid of 7mg/dl or more in men or 6mg/dl or more in women
Eligibility Criteria
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Inclusion Criteria
2. Metabolic syndrome
Exclusion Criteria
2. Severe valvular heart disease
3. Significant structure heart diseases such as hypertrophic, dilated, infiltrative or restrictive cardiomyopathy, or congenital heart disease
4. Persistent or chronic atrial fibrillation
5. Status post cardiac surgery, including coronary artery bypass surgery of valve intervention
6. Status post intra-cardiac device implantation
7. Chronic obstructive pulmonary disease
8. Severe anemia
9. An obvious systemic disease that interferes left ventricular diastolic dysfunction such as acute coronary syndrome
20 Years
75 Years
ALL
No
Sponsors
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National Defense Medical Center, Taiwan
OTHER
Responsible Party
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Cheng-Wei Liu
Cardiologist
Principal Investigators
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Cheng-Wei Liu, M.D.
Role: PRINCIPAL_INVESTIGATOR
Tri-service General hospital, Songshan branch, National defense medical center
Locations
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Tri-service General Hospital, songshan branch
Taipei, Songshan Dist., Taiwan
Countries
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Other Identifiers
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2-106-05-078
Identifier Type: -
Identifier Source: org_study_id
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