Lipid Metabolism Disorders Clinical Trial
— CHOKOOfficial title:
Cholesterol Effects of Kori-tofu Proteins
Verified date | December 2021 |
Source | Wageningen University and Research |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The study is a randomized, cross-over, double-blind, controlled trial in which participants with mildly elevated levels of cholesterol will receive two 4-week interventions (e.g. kori-tofu or control), with a wash-out period of 4 weeks in between. During the intervention periods, subjects will eat 3 slices of bread per day, representing a Kori-tofu dose of 34.5 grams or a matched reference. Fasting total and LDL cholesterol will be determined at the start and end of each of the two intervention periods.
Status | Completed |
Enrollment | 48 |
Est. completion date | December 7, 2021 |
Est. primary completion date | December 7, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 40 Years to 70 Years |
Eligibility | Inclusion Criteria: - Age between 40-70 years; - BMI between 18.5-35 kg/m2; - Total cholesterol levels >5 mmol/L or LDL >3 mmol/L Exclusion Criteria: - Use of medication/supplements/food items that may influence the study results, such as cholesterol lowering medication, Becel ProActiv (judged by our research physician); - Total cholesterol levels >7 mmol/L; - LDL cholesterol levels >5 mmol/L; - Reported slimming, medically prescribed or other extreme diets; - Reported weight loss or weight gain of >5 kg in the month prior to pre-study screening; - Not willing to give up blood donation during the study; - Current smokers; - Alcohol intake =4 glasses of alcoholic beverages per day; - Pregnant, lactating or wishing to become pregnant in the period of the study (self-reported); - Abuse of soft and/or hard drugs; - Food allergies or intolerances for products that we use in the study; - Participation in another clinical trial at the same time; NL75320.081.20 CHOKO Version number: 4, April 2021 15 of 34 - Being an employee of the Food, Health & Consumer Research group of Wageningen Food & Biobased Research. |
Country | Name | City | State |
---|---|---|---|
Netherlands | Wageningen University & Research | Wageningen | Gelderland |
Lead Sponsor | Collaborator |
---|---|
Wageningen University and Research | Asahimatsu Foods |
Netherlands,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in total cholesterol levels | under fasting conditions | 0 weeks, 4 weeks, 8 weeks and 12 weeks | |
Primary | Change in LDL cholesterol levels | under fasting conditions | 0 weeks, 4 weeks, 8 weeks and 12 weeks | |
Secondary | Change in HDL cholesterol levels | under fasting conditions | 0 weeks, 4 weeks, 8 weeks and 12 weeks | |
Secondary | Change in triglycerides levels | under fasting conditions | 0 weeks, 4 weeks, 8 weeks and 12 weeks | |
Secondary | Change in leptin levels | under fasting conditions | 0 weeks, 4 weeks, 8 weeks and 12 weeks | |
Secondary | Change in adiponectin levels | under fasting conditions | 0 weeks, 4 weeks, 8 weeks and 12 weeks | |
Secondary | Change in plasma insulin levels | under fasting conditions | 0 weeks, 4 weeks, 8 weeks and 12 weeks | |
Secondary | Change in HbA1c levels | under fasting conditions | 0 weeks, 4 weeks, 8 weeks and 12 weeks | |
Secondary | Change in fructosamine levels | under fasting conditions | 0 weeks, 4 weeks, 8 weeks and 12 weeks | |
Secondary | Change in glucose levels | under fasting conditions | 0 weeks, 4 weeks, 8 weeks and 12 weeks | |
Secondary | Change in systolic blood pressure levels | under fasting conditions | 0 weeks, 4 weeks, 8 weeks and 12 weeks | |
Secondary | Change in diastolic blood plessure levels | under fasting conditions | 0 weeks, 4 weeks, 8 weeks and 12 weeks |
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