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Pilot study to assess the effect of Brazil nuts on plasma selenium levels in healthy male volunteers aged 65 years and over

Not Applicable
Not yet recruiting
Conditions
Healthy male volunteers aged 65 years and older. The health condition for which the intervention may be indicated is prostate cancer.
Cancer - Prostate
Registration Number
ACTRN12614001092684
Lead Sponsor
The University of Queensland
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Not yet recruiting
Sex
Male
Target Recruitment
30
Inclusion Criteria

Eligible participants include healthy, non-smoking men aged 65 years and older

Exclusion Criteria

Ineligible participants include the presence of nut-allergies and the regular use of a selenium supplement and not willing to discontinue use during the research study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The change in mean selenium response from baseline to 30 days[A blood sample (60 mL of whole blood) will be collected on 3 occasions: at baseline (day 0), midpoint (day 15) and endpoint (day 30) of the intervention. Plasma selenium levels will be assessed.]
Secondary Outcome Measures
NameTimeMethod
utritional biomarkers: plasma and whole blood GPx [The primary outcome blood sample will also be used to measure the secondary outcomes. A blood sample (60 mL of whole blood) will be collected on 3 occasions: at baseline (day 0), midpoint (day 15) and endpoint (day 30) of the intervention.];Selenoprotein P<br>[The primary outcome blood sample will also be used to measure the secondary outcomes. A blood sample (60 mL of whole blood) will be collected on 3 occasions: at baseline (day 0), midpoint (day 15) and endpoint (day 30) of the intervention.];Inflammatory marker: C-reactive protein (CRP)[The primary outcome blood sample will also be used to measure the secondary outcomes. A blood sample (60 mL of whole blood) will be collected on 3 occasions: at baseline (day 0), midpoint (day 15) and endpoint (day 30) of the intervention.]
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