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Effect of probiotic cheese on blood indices and intestinal microflora of healthy volunteers and elderly individuals

Completed
Conditions
Blood indices and intestinal microflora
Digestive System
Improving intestinal flora
Registration Number
ISRCTN15061552
Lead Sponsor
Healthy Dairy Products Ltd (Estonia) - Bio-Competence Centre
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
210
Inclusion Criteria

1. Wish to participate in the study
2. Aged 18 years and over (group I), aged over 60 (Group II), either sex
3. Healthy (i.e. no known health problems and no medical conditions that require drug therapy)
4. Signed informed consent

Exclusion Criteria

1. History of any gastrointestinal disease
2. Use of any antimicrobial drug within last month
3. Use of any regular concomitant medication, including medical preparations
4. Food allergy
5. Pregnancy or breastfeeding (Group I)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Group I: <br>Blood, urine and faecal samples are collected at the recruitment, after 3 weeks of probiotic treatment, after a 2-week wash-out period and after a 3-week placebo treatment. The survival of the probiotic strain in gastrointestinal tract (GIT) and its effect on intestinal microflora and clinical blood indices of healthy volunteers is measured.<br><br>Group II: <br>At the recruitment and 6 hours after cheese consumption the arterial elasticity will be assessed. After 6 hours another blood sample is collected and after 4 days the whole procedure is repeated.
Secondary Outcome Measures
NameTimeMethod
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