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Lipid-lowering Effect of Plant Stanol Drink

Not Applicable
Completed
Conditions
Hypercholesterolemia
Registration Number
NCT01716390
Lead Sponsor
Raisio Group
Brief Summary

To determine the effect of investigational products on serum LDL cholesterol.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
56
Inclusion Criteria
  • healthy mildly to moderate hypercholesterolemic (serum total cholesterol 5.2-8.5 mmol/l) adults
  • signed written informed consent
Exclusion Criteria
  • participation in a clinical study within 30 days prior to screening visit and throughout the study
  • severe obesity
  • consumption of lipid/cholesterol lowering medication 1 month prior to the screening visit and throughout the study
  • consumption of plant stanol or plant sterol containing food products such as Benecol or Becel pro active 1 month prior to visit 2

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Change in serum LDL cholesterol0 vs 4 weeks
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Good Food Practice

🇸🇪

Uppsala, Sweden

Good Food Practice
🇸🇪Uppsala, Sweden

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