Lifestyle Clinical Trial
Official title:
Bioavailability of Omega-3 Long-chain Polyunsaturated Fatty Acids (LCPUFA) From Foods Enriched With Vegetable-encapsulated Omega-3 Oils
CSIRO's Food Program has developed a novel vegetable-based Omega-3 long-chain polyunsaturated fatty acid (Omega 3)encapsulant to be used as ingredient in various food products, however, it is unknown whether the vegetable-based carrier matrix will affect omega-3 bioavailability. This project aims to compare the bioavailability of omega-3 from two test foods containing vegetable (cauliflower)-encapsulated algal oil (the "ingredient") against a control test product (algal oil gel capsules) across two ethnicities (Australian European vs. Chinese Singaporean).
Status | Recruiting |
Enrollment | 24 |
Est. completion date | February 2021 |
Est. primary completion date | February 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 21 Years to 50 Years |
Eligibility | Inclusion Criteria: - Healthy men - Age: 21-50 years old - BMI 18-27.5 kg/m2 - Consume less than 2 meals of fatty fish/week - Not consume fish oil supplements over the past 3 months - Identify as Australian European in ethnicity (Australian with European heritage) for Australian arm of study - Identify as Chinese Singaporean in ethnicity (Singaporean with Chinese heritage) for Singaporean arm of study Exclusion Criteria: - History of chronic disease - cancer, type 2 diabetes, cardiovascular disease, liver disease or any condition that may, in the opinion of the principle investigator, influence the study outcomes (Self reported, no clinical testing will be performed) - History of gastrointestinal disease, pancreatic insufficiency, conditions resulting in fat malabsorption - chronic pancreatitis, cystic fibrosis, coeliac disease, Crohns disease, gastric bypass surgery, small bowel resection, abnormal thyroid function (Self reported, no clinical testing will be performed) - Bleeding disorders, currently taking anticoagulants or has received anticoagulants within 28 days of Day 1 of the trial, with the exception of low dose aspirin up to150 mg daily (Self reported) - Any medical procedures deemed by the principal investigator to affect study outcomes - Known food allergies, hypersensitivity, dietary avoidance or intolerance to the study foods - Taking medications/supplements known to influence lipid metabolism and gastric emptying - On any weight-loss program - History of smoking during the 6 months prior to the study (Self reported) - Persons considered by the investigator to be unwilling, unlikely or unable to comprehend or comply with the study protocol - History of drug abuse or alcoholism (Self reported) - Participation in another research study within 30 days preceding the start of this study |
Country | Name | City | State |
---|---|---|---|
Australia | CSIRO, Health and Biosecurity | Adelaide | South Australia |
Singapore | A*STAR | Singapore |
Lead Sponsor | Collaborator |
---|---|
Commonwealth Scientific and Industrial Research Organisation, Australia | Agency for Science, Technology and Research |
Australia, Singapore,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Blood Plasma Omega-3 Concentration | Blood Plasma Omega-3 Concentration | 0 Minutes (T0), 120 Minutes (T1), 240 Minutes (T2), 360 Minutes (T3), 480 Minutes (T4) and 1440 Minutes (T5) |
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