Compare Effects of a Soluble Fiber on Weight and Blood Cholesterol

Completed · Not applicable

Conditions studied: Obesity

In brief

Obesity and type 2 diabetes have clearly been linked together and identified as epidemics in much of the developed world. Historically several different dietary fibers have been used as means of reducing body weight and the related development of type 2 diabetes. These studies have generated mixed, if not inconsistent, results suggesting that none of these fibers promise a solution to either of these two conditions. We are proposing to investigate the effects of including a new soluble fiber, a-cyclodextrin, FBCx® (to be called Y288 in this study), into the diet of adult overweight volunteers.

Key facts

Study ID

NCT00682916

Run by

University of California, Davis

People needed

42

Starts

2007-04-01

Expected to finish

2008-12-01

Last updated by the study team

2017-05-30

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 30 men and 30 women
• Age 18- 65 years
• BMI 25.0 - 32.0 Kg/m²
• fasting glucose <126 mg/dL
• Blood pressure < 140/85 mm Hg. Hypertension on stable drug regimen using 2 or fewer antihypertensives will be acceptable.
• Total plasma cholesterol <240 mg/dl, LDL-cholesterol <160 and triglycerides <400 mg/dl. Hyperlipidemia on a stable medication regimen using single anti-hyperlipidemic drug acceptable.

You may not qualify if…

• Pregnant women, women who plan to become pregnant during the study period
• Women who have given birth within the previous 12 months
• Lactating women
• History or presence of Type 2 diabetes; kidney disease; (creatinine >1.4); liver disease (X2 fold increase in AST or ALT); gout; cancer; untreated thyroid disease; gastrointestinal disease; other metabolic diseases or malabsorption syndromes
• Habitual low-fat intake (less than 20%)
• History of eating disorder
• Subjects who have lost 10% of body weight within the last 12 months or who plan to initiate a weight loss program
• Use of prescription or over-the counter anti-obesity medications or supplements (phenylpropanolamine, ephedrine, caffeine) for at least 6 months prior of study.
• Subjects with pacemakers will not participate in bioimpedance studies but will go through all the other testing.

Where it is running

• UC Davis — Sacramento, California, United States

Full record on ClinicalTrials.gov

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