Obesity Clinical Trial
Official title:
Effects of Different Types of Carbohydrates in Snacks and Beverages on Glycemia, Insulinemia and Appetite.
Verified date | August 2021 |
Source | Clinical Nutrition Research Centre, Singapore |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The aim of the study is to describe the glycemic, insulinemic and appetitive responses to liquid and solid foods where either soluble fiber or maltodextrin are used as the carbohydrate substrate.
Status | Completed |
Enrollment | 23 |
Est. completion date | July 21, 2020 |
Est. primary completion date | July 21, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 21 Years to 60 Years |
Eligibility | Inclusion Criteria: - Healthy Chinese male subjects aged between 21 and 60 years - Either one of the three criteria: - Normal weight (body mass index 18.5-22.9 kg/m2) and Fasting Blood Glucose 5.0-6.0mmol/L - Overweight (body mass index 23.0 - 30.0 kg/m2) and Fasting Blood Glucose 5.0-6.0mmol/L - Overweight (body mass index 23.0 - 30.0 kg/m2) and Fasting Blood Glucose <5.0mmol/L Exclusion Criteria: - Do smoke - Have any metabolic diseases (such as diabetes, hypertension etc) - Have known glucose-6-phosphate dehydrogenase deficiency (G6PD deficiency) - Have medical conditions and/or taking medications known to affect glycemia (glucocorticoids, thyroid hormones, thiazide diuretics) - Have any major organ dysfunction (e.g. cardiovascular, respiratory, hepatic, renal, gastrointestinal) that may influence taste, olfaction, appetite, digestion, metabolism, absorption or elimination of test foods, nutraceutical or drug - Consume fiber supplements or other supplements that is likely to interfere with study outcomes - Have any severe food allergy (e.g. anaphylaxis to peanuts) - Have any known allergies to any food components of the study protocol - Have active Tuberculosis (TB) or currently receiving treatment for TB - Have any known Chronic infection or known to suffer from or have previously suffered from or is a carrier of Hepatitis B Virus (HBV), Hepatitis C Virus (HCV), Human Immunodeficiency Virus (HIV) - Is a study team member or an immediate family of any study team member. Immediate family member is defined as a spouse, parent, child, or sibling, whether biological or legally adopted. - Is enrolled in a concurrent research study judged not to be scientifically or medically compatible with the study of the CNRC. - Partake in sports at the competitive and/or endurance levels - Intentionally restrict food intake - Have poor veins impeding venous access - Have any history of severe vasovagal syncope (blackouts or near faints) following blood draws |
Country | Name | City | State |
---|---|---|---|
Singapore | Clinical Nutrition Research Centre | Singapore |
Lead Sponsor | Collaborator |
---|---|
JeyaKumar Henry | Tate and Lyle Ingredients France |
Singapore,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in plasma blood glucose from fasting baseline value (Time Frame: Up to 180 minutes). | Blood plasma glucose measured at 0, 15, 30, 45, 60, 90, 120, 150 and 180mins after meal ingestion. | up to 180 minutes | |
Primary | Change in plasma blood insulin from fasting baseline value (Time Frame: Up to 180 minutes). | Blood plasma insulin measured at 0, 15, 30, 45, 60, 90, 120, 150 and 180mins after meal ingestion. | up to 180 minutes | |
Secondary | Change in subjective appetite ratings from fasting baseline value (Time Frame: Up to 180 minutes). | Appetite ratings measured at 0, 15, 30, 45, 60, 90, 120, 150 and 180mins after meal ingestion. | up to 180 minutes |
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