Status:
COMPLETED
Pharmacokinetics and Pharmacodynamics of Fructose
Lead Sponsor:
University of Florida
Conditions:
Healthy
Eligibility:
All Genders
18+ years
Brief Summary
The purpose of this study is to determine whether sucrose vs high fructose corn syrup from a soft drink results in differences in various metabolic byproducts such as fructose, glucose, serum uric aci...
Detailed Description
Fructose consumption has risen sharply during the past several decades. Since its introduction to the United States in 1967, high fructose corn syrup (HFCS) has overtaken sucrose as the main sweetener...
Eligibility Criteria
Inclusion
- adult subjects aged 18 years or older
- either gender
- any ethnicity
- willing to abstain from drinking any alcohol 3 days prior to a study visit
Exclusion
- history of liver or kidney disease
- history of diabetes mellitus or fasting blood glucose ≥ 126 mg/dl or random blood glucose ≥ 200 mg/dl
- currently taking any medication (except oral contraceptives)
- consume more than 1 alcoholic drink per day
- pregnant or breast-feeding
- blood donor in the previous 8 weeks
- history of gout
Key Trial Info
Start Date :
March 1 2008
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
August 1 2010
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT00661947
Start Date
March 1 2008
End Date
August 1 2010
Last Update
February 16 2012
Active Locations (1)
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1
University of Florida, Department of Pharmacy Practice, Center for Pharmacogenomics
Gainesville, Florida, United States, 32610