CompletedPhase 4ACTRN12607000345482

The potential of selenium supplements provided as selenium-enriched dairy protein or yeast selenium to improve selenium status


Sponsor

Professor Graeme Young MD, FRACP

Enrollment

20 participants

Start Date

Nov 20, 2007

Study Type

Interventional

Conditions

Summary

It is proposed to evaluate a selenised dairy product with regard to its safety and influence on selenium status, using plasma and rectal biomarkers. It will be compared for its efficacy & bioavailability with a selenium yeast product.


Eligibility

Sex: Both males and femalesMin Age: 50 Yearss

Plain Language Summary

Simplified for easier understanding

This study investigates the potential of selenium supplements provided as selenium-enriched dairy protein or yeast selenium to improve selenium status. It is looking for both men and women, aged 50 and older who have healthy, with no active bowel disease, orWith a previous history of adenoma removal >6 months ago, With plasma selenium at or below 100 µg/dL. (t.... If you are interested, you may need to attend study visits and follow the research team's instructions.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

It is proposed to evaluate a selenised dairy product (Tatura Bio Se®, TMI Victoria) in a human intervention study with regard to its safety and influence on selenium status, using plasma and rectal b

It is proposed to evaluate a selenised dairy product (Tatura Bio Se®, TMI Victoria) in a human intervention study with regard to its safety and influence on selenium status, using plasma and rectal biomarkers. A group of >50 year old volunteers considered at-risk for colon cancer by virtue of age and/or other standard risk factors. Particpants will commence with a wash out period of 2-4 wks instructing them not to add selenium products to their diet 10 participants will be allocated Se Milk Protein Concentrate 150µg/d and a different group of 10 will be allocated Selplex 150µg/d at the same time i.e to run in parallel Each participant will undertake a follow on wash out period of 6 weeks. Blood samples will be taken every 2 weeks throughout the intervention and wash out periods Rectal pinch biopsies will be performed for bowel tissue samples at the beginning and end of each intervention and at the end of the follow-on washout period.


Locations(1)

Australia

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ACTRN12607000345482