Clinical Trials Directory

Trials / Completed

CompletedNCT00616057

Evaluation of Fructans Supplementation on Parameters of Metabolic Syndrome

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
34 (actual)
Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain · Academic / Other
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Obesity is constantly increasing, causing an important risk to develop diseases such as heart disease, diabetes,... Some recent studies have shown that obese people present modifications of colon microflora and a low-grade inflammation. In our laboratory, we have demonstrated that the intake of fructans lessens dietary intake, body weight gain, adipose tissue accumulation and steatosis in rodents. These effects lead to an improvement of insulin resistance and hyperglycemia in diabetic rats and mice. Fructans are also able to restore the microflora disturbed by a high fat diet and to prevent endotoxemia. Moreover, studies have shown that fructans intake promotes satiety (Cani et al, Diabetes 2007) and or decreases fat mass (Abrams et al, Journal of Pediatrics 2007) in healthy human. An intervention study in obese patients is thus needed to study the effects of fructans in the target population.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTSynergy 18 grams/day during the first week and then 8 grams twice a day during 3 months
DIETARY_SUPPLEMENTmaltodextrin8 grams/day during the first week and then 8 grams twice a day during 3 months

Timeline

Start date
2008-02-01
Primary completion
2010-05-01
Completion
2011-06-01
First posted
2008-02-15
Last updated
2012-07-06

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT00616057. Inclusion in this directory is not an endorsement.