Dose Response Study of a Fermented Yogurt on the Immune System and Gut Health (PRO)
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
The purpose of this study is to determine the dose-response effect of a yogurt containing a combination of bifidobacterium Lactis (BB-12) and Lactobacillus Acidophilus (LA-5) and green tea extract on markers of the immune system and gut health in healthy subjects. We hypothesize that the response of the immune function will be dose-dependent of the probiotics found in the fermented yogurt.
| Condition | Intervention |
|---|---|
|
Immune System |
Dietary Supplement: Yogurt with 1X10E9 BB-12 and LA-5 Dietary Supplement: Yogurt with 1X10E10 BB-12 and LA-5 Dietary Supplement: Yogurt Placebo |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator, Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | Dose Response Study of the Impact of a Yogurt Containing Bifidobacterium Lactis BB-12 and Lactobacillus Acidophilus LA-5 on the Immune System and Gut Health. |
- Phagocytosis activity and oxidative metabolism in phagocytes. [ Time Frame: 6 weeks after vaccination ] [ Designated as safety issue: No ]
- antipneumococcics antibody specific serotype response to S. pneumoniae vaccination. [ Time Frame: 6 weeks after yogurt consumption and vaccination ] [ Designated as safety issue: No ]
- Intestinal microflora characteristics. [ Time Frame: 4 weeks after yogurt consumption ] [ Designated as safety issue: No ]
- Influence of blood lipids. [ Time Frame: After 4 weeks and 10 weeks of yogurt consumption ] [ Designated as safety issue: No ]
| Enrollment: | 58 |
| Study Start Date: | August 2008 |
| Study Completion Date: | May 2009 |
| Primary Completion Date: | December 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
L.acidophilus and B.lactis (1x10E9 of each probiotics) with 40 mg of green the extract
|
Dietary Supplement: Yogurt with 1X10E9 BB-12 and LA-5
100g of yogurt containing the probiotics L.acidophilus and B.lactis (concentrations of 1x10E9 of each probiotics) with 40 mg of green tea extract, once a day for 10 weeks.
|
|
Experimental: 2
L.acidophilus and B.lactis (1x 10E10 of each probiotics) with 40 mg of green tea extract
|
Dietary Supplement: Yogurt with 1X10E10 BB-12 and LA-5
100g of yogurt containing the probiotics L.acidophilus and B.lactis (concentrations of 1x10E10 of each probiotics) with 40 mg of green tea extract, once a day for 10 weeks.
|
|
Placebo Comparator: 3
Placebo
|
Dietary Supplement: Yogurt Placebo
100g of yogurt placebo containing no probiotics and no green tea extract, once a day for 10 weeks.
|
Detailed Description:
There is an increasing list of food containing probiotics on the market. Several studies have emphasized the health benefits of single probiotics, particularly on the immune system. However, it is unclear how a combination of two different probiotics complemented with green tea extract can beneficially modify markers of the immune.
The aim of this study is to determine the dose-response effect of a yogurt containing a combination of bifidobacterium lactis (BB-12) and Lactobacillus Acidophilus LA-5 and green tea extract on immune system in healthy subjects. More specifically, this randomized, parallel placebo controlled study will investigate the impact of increasing doses (109 and 1010) of these probiotics on phagocytosis activity, oxidative metabolism and on the antipneumococcics antibody specific serotype response S. pneumoniae vaccination. Finally, this study will also examine the effect of increasing dose of these probiotics on intestinal microflora and blood lipids.
Eligibility| Ages Eligible for Study: | 18 Years to 55 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Age between 18 to 55 years
- Healthy individuals, non-smokers
- BMI between 18 and 35 kg/m2
- Stable weight (+/- 5kg) for 3 months before randomisation
- Agree to receive a vaccine Pneumovax 23®
Exclusion Criteria:
- Pregnant or lactating woman
- Previous history of cardiovascular disease
- Diabetes
- Kidney or liver disease
- Gastrointestinal disorders or diseases
- Endocrine disorders or diseases
- Allergy
- Subjects taking hypolipidemic drugs, antidepressant, medication for high blood pressure, for inflammation or auto-immune diseases.
- Subject who have receive antipneumococcics vaccine in the year before randomisation.
Contacts and Locations| Canada | |
| Institute of Nutraceuticals and Functional Foods (INAF), Laval University | |
| Quebec, Canada, G1V 0A6 | |
| Principal Investigator: | Benoît Lamarche, PhD | Institute of Nutraceuticals and Functional Foods (INAF), Laval University. |
| Study Director: | Jacques Hébert, MD | Faculty of Medicine, Laval University. |
More Information
Publications:
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Benoît Lamarche, Study Principal Investigator, Institute of Nutraceuticals and Functional Foods (INAF), Laval University |
| ClinicalTrials.gov Identifier: | NCT00730626 History of Changes |
| Other Study ID Numbers: | INAF-119 |
| Study First Received: | August 6, 2008 |
| Last Updated: | June 19, 2009 |
| Health Authority: | Canada: Health Canada |
Keywords provided by Laval University:
|
Probiotics Immunity Immune response |
Intestinal microflora Blood lipids Phagocytosis activity |
ClinicalTrials.gov processed this record on June 18, 2013