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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COMPLETED
220 participants
OBSERVATIONAL
2003-01-31
2005-12-31
Brief Summary
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Detailed Description
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Outcome will be determined by examining Dexa Scan data and surrogate clinical endpoints. The clinical endpoints include: anthropometric measurements, Dexa analysis, bioelectric impedance, and BP measurements, and the biochemical measures of: lipid profile, fasting insulin and glucose, liver functions and uric acid levels.
Conditions
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Keywords
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Study Design
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DEFINED_POPULATION
OTHER
Eligibility Criteria
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Inclusion Criteria
* Male and female
* Non-diabetic
* Resident of Dunedin and Invercargill
Exclusion Criteria
18 Years
68 Years
ALL
Yes
Sponsors
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Edgar National Centre for Diabetes Research
OTHER
Principal Investigators
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Jim I Mann, FRACP, PhD
Role: STUDY_DIRECTOR
Edgar National Centre for Diabetes Research
Locations
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Edgar National Centre for Diabetes Research
Dunedin, Otago, New Zealand
Countries
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Related Links
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Edgar National Centre for Diabetes Research, NZ website
Other Identifiers
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ENCDR_3
Identifier Type: -
Identifier Source: org_study_id