Clinical Trials Directory

Trials / Completed

CompletedNCT01846117

Once-Daily Oral Dose of BeneFlax to Healthy Older Adults

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
32 (actual)
Sponsor
University of Saskatchewan · Academic / Other
Sex
All
Age
60 Years – 80 Years
Healthy volunteers
Accepted

Summary

The investigators are investigating whether the flax lignan, secoisolariciresinol diglucoside, decreases oxidative stress and inflammation. The flax seed lignan is believed to be broken down in the body to produce the health benefits of flax. Flax lignan is separated from the whole flax seed as this compound is believed to have health effects. Decreasing oxidative stress and inflammation should improve a number of the problems associated with aging. This intervention consists of 600 milligrams of the flax lignan SDG daily or an equivalent amount of whey protein. The investigators are comparing lignan to a placebo (whey powder) to examine whether a dietary intervention (i.e. flax seed containing lignan) might decrease oxidative stress and inflammation.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTsecoisolariciresinol diglucoside, vitamin DSDG supplementation as a packet of 1.6g/day of BeneFlax containing 600 mg SDG for 24 weeks Vitamin D Natural Product Number (NPN) 80003663 WN Pharmaceuticals Natural Factors Whey Factors

Timeline

Start date
2013-04-01
Primary completion
2014-11-01
Completion
2014-11-01
First posted
2013-05-03
Last updated
2018-06-14

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01846117. Inclusion in this directory is not an endorsement.