RecruitingACTRN12611000012976

Microencapsulation for Enhanced Bioavailability of Fish Oil - Acute Study

Microencapsulation for Enhanced Bioavailability of Fish Oil in Healthy Adult Volunteers - Acute Study


Sponsor

CSIRO Preventative Health Flagship

Enrollment

15 participants

Start Date

Oct 18, 2010

Study Type

Interventional

Conditions


Eligibility

Sex: Both males and femalesMin Age: 18 YearssMax Age: 70 Yearss

Inclusion Criteria5

  • Male and Females aged between 18-70 years
  • Normal dietary habits (no medically prescribed diet, no slimming diet, and no vegan or macrobiotic diet).
  • Body Mass Index >18 kg/m2 < 35kg/m2
  • Apparently healthy: no reported current or previous metabolic diseases, gastrointestinal disorders, renal or cardiovascular disease.
  • Person having given their specific consent in writing.

Exclusion Criteria8

  • Regular use of supplements containing omega-3 essential fatty acids must have ceased 2 months prior to the start of the study.
  • Regular consumption of foods supplemented with omega-3 essential fatty acids such as some breads and milk products
  • Consumption of fish as part of regular dietary patterns
  • Current relevant medical treatment (subject to judgement of the investigator).
  • High alcohol consumption (>21 standard drinks/week)
  • Reported participation in another biomedical trial 3 months before the start of the study or during the study.
  • Food allergies or intolerances (dairy, lactose, peanuts, shellfish, etc…).
  • Recent history (within 12 months) of substance abuse including alcohol abuse.

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Interventions

This study will compare the short term bioavailability of 3 delivery systems containing omega-3 oils. They are (1) gel capsules versus (2) MicroMAX 1 powder – formulated with milk protein-sugar versus

This study will compare the short term bioavailability of 3 delivery systems containing omega-3 oils. They are (1) gel capsules versus (2) MicroMAX 1 powder – formulated with milk protein-sugar versus (3) MicroMAX powder - formulated with milk protein-sugar-resistant starch) when combined with a flavoured milk in individuals. Bioavailability will be assessed by measurement of EPA & DHA in blood/plasma. This is a crossover design study in which all participants will receive the three treatments with a washout period of 6 weeks between each treatment. To investigate the bioavailability of a single dose of omega-3 oils delivered via the three above mentioned formats over 48 hrs. The two different MicroMAX powders (one formulated with milk protein-sugar and other milk protein-sugar-resistant starch) will each be provided as an 8g serve containing a dose of 500mg/g omega-3 oil. The gel capsules will be given as a one-off dose of 4 capsules (each capsule will contain 1000mg of omega-3 oil).


Locations(1)

Australia

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ACTRN12611000012976