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Plant Stanol Ester Beverage and Ileostoma Patients

Not Applicable
Completed
Conditions
Ileostoma
Registration Number
NCT00846937
Lead Sponsor
University of Helsinki
Brief Summary

We aim to examine efficacy of a plant stanolester beverage to lower serum cholesterol and LDL-cholesterol levels, when given with or without a fatty acid preparation. Study subjects are otherwise healthy proctocolectomized ileostoma patients (n=10), who consume stanolester beverage with or without a fatty acid preparation in a random order for one week period after a standardized low-fat meal. Washout period is 4 weeks. Serum lipids, lipoprotein lipids, sterols and fecal sterols and variables of cholesterol metabolism will be examined accordingly.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
10
Inclusion Criteria
  • healthy proctocolectomized subjects with an ileostoma
Exclusion Criteria
  • Chronic illness

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Primary Outcome Measures
NameTimeMethod
serum cholesterol levelAfter treatment perdiods
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Helsinki, Department of Medicine

🇫🇮

Helsinki, Finland

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