Diabetes Clinical Trial
Official title:
Glycemic and Insulinemic Response of Pasta Products in Comparison to Asian
| NCT number | NCT03646812 |
| Other study ID # | 2018/00622 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | August 10, 2018 |
| Est. completion date | June 1, 2020 |
| Verified date | August 2023 |
| 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 determine the glycaemic and insulinaemic index of pasta products and local foods. It is hypothesized that different pasta cuts and wholegrain composition of pasta and local foods have different GI depending on the nature of the carbohydrate content and the food structure within each food.
| Status | Completed |
| Enrollment | 32 |
| Est. completion date | June 1, 2020 |
| Est. primary completion date | June 1, 2020 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 21 Years to 40 Years |
| Eligibility | Inclusion Criteria: - Healthy Asian - Indian and Chinese ethnicity - Age between 21-40 years - Body mass index between 18.5 to 25 kg/m2 - Normal blood pressure (<140/90 mmHg) - Fasting blood glucose < 6 mmol/L Exclusion Criteria: - Is a current smoker - Is currently pregnant - 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 - 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. - enrolled in a concurrent research study judged not to be scientifically or medically compatible with the study. - Have partake in sports at the competitive and/or endurance levels - Have intentionally restrict food intake |
| Country | Name | City | State |
|---|---|---|---|
| Singapore | Clinical Nutrition Research Centre | Singapore |
| Lead Sponsor | Collaborator |
|---|---|
| Clinical Nutrition Research Centre, Singapore | Barilla Singapore Pte Ltd |
Singapore,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Glucose | Blood will be collected and measured using hemocue analyzer. | up to 180 minutes | |
| Primary | Insulin | Blood will be collected and measured using COBAS analyzer. | up to 180 minutes |
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