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Clinical Trial Summary

The study will enroll 68 overweight male and female subjects with a high (> 2 3dl-can soda/day) consumption of sweetened beverage per day. After a run-in period of 4 weeks, subjects will be randomized to either a 12-week intervention arm in which sweetened beverages will be replaced by artificially sweetened, calorie-free beverages, or to a control arm. The following measurements will be performed at the end of the run-in period and at the end of the intervention period

- intrahepatic fat concentration

- visceral fat volume

- changes in day-long metabolic profile from baseline(plasma glucose, insulin, and triglyceride concentrations)

- changes in food intake and daily energy, carbohydrate and sugars intake from baseline


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT01394380
Study type Interventional
Source University of Lausanne
Contact
Status Completed
Phase N/A
Start date October 2011
Completion date April 2014

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