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Plant Stanol Ester Beverage and Ileostoma Patients (STOMA)

U

University of Helsinki

Status

Completed

Conditions

Ileostoma

Treatments

Dietary Supplement: Plant stanolester and fatty acid

Study type

Interventional

Funder types

Other

Identifiers

NCT00846937
3097
U1010G0020

Details and patient eligibility

About

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.

Enrollment

10 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • healthy proctocolectomized subjects with an ileostoma

Exclusion criteria

  • Chronic illness

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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