Pharmacokinetics and Pharmacodynamics of Fructose
Completed
Conditions studied: Healthy
In brief
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 acid, triglyceride and lactate.
Key facts
- Study ID
- NCT00661947
- Run by
- University of Florida
- People needed
- 40
- Starts
- 2008-03-01
- Expected to finish
- 2010-08-01
- Last updated by the study team
- 2012-02-16
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- 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
You may not qualify if…
- 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
Where it is running
- University of Florida, Department of Pharmacy Practice, Center for Pharmacogenomics — Gainesville, Florida, United States
Full record on ClinicalTrials.gov
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