- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05401604
Probiotic Beer to Enhance Gut Health and Immune System Function (PBEER)
May 27, 2022 updated by: Mei Hui Liu, National University, Singapore
This study investigates the immunological and gut microbiome effects of moderate probiotic beer consumption.
Study Overview
Status
Completed
Conditions
Detailed Description
Studies have shown that moderate alcohol consumption and probiotics have each shown immunomodulatory anti-inflammatory effects.
However, to our knowledge, the effect of adding a probiotic strain to a beer drink, together with moderate alcohol consumption, on immunity and gut microbiome has yet to be studied.
The probiotic beer used in this study taps on this unexplored research area and may potentially serve as a more healthful option to consumers than normal beer in the future, given the vast popularity of this beverage and probiotics.
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Singapore, Singapore, 118177
- National University of Singapore
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Ability to give informed consent.
- 21 - 60 years of age (inclusive) at screening.
- Healthy male, as determined by medical history, physical examination and laboratory results within normal reference range for the population or investigator site, or results with acceptable deviations that are judged to be not clinically significant by the investigator.
- Race must be Chinese.
- Willing to consume 1 beer can per day for 14 days.
- Not on any regular medications (western/ traditional).
- No family history of alcoholism.
Exclusion Criteria:
- Female.
- A current smoker, have smoked, or is a user of tobacco products for the past 2 years.
- History or presence of current lipid and cardiovascular disorders, respiratory, hepatic, renal, gastrointestinal, endocrine, lipid disorder, haematological, malignancy or neurological disorders capable of significantly altering the performance of the biomarker panel; or of interfering with the interpretation of data.
- History of alcoholism, alcohol dependence, alcohol abuse, alcohol allergy and/or any other alcohol use disorders.
- History of Type 1/ Type 2 diabetes and use of anti-diabetic medications in the past.
- Regular use of medication that are known to have an effect on immune function.
- Regular use of aspirin.
- A naïve alcohol drinker.
- Persons with known or ongoing psychiatric disorders or drug abuse within 3 years.
- Active infection requiring systemic antiviral or antimicrobial therapy that will not be completed prior to first visit of the study.
- Treatment with any investigational drug, or biological agent within one (1) month of screening or plans to enter into an investigational drug/ biological agent study during the duration of this study.
- Significant change in weight (+/- 5%) during the past month.
- Antibiotic use in the past 2 months.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Moderate probiotic beer consumption
1 can of 330ml (3.5-5% alcohol) probiotic beer.
Ingredients: water, grains, raspberry puree, yeast, and lactic acid bacteria (Lactobacillus paracasei Lpc-37®, or Lactobacillus paracasei LAFTI®L26).
|
Consumption of one can of probiotic beer per day for 14 days.
Blood and fecal samples will be collected at the start and end of the intervention to analyse for immunological biomarkers and gut microbiome.
|
|
Placebo Comparator: Moderate normal beer consumption
1 can of 330ml (3.5-5% alcohol) normal beer.
Ingredients: water, grains, raspberry puree, and yeast.
|
Consumption of one can of normal beer per day for 14 days.
Blood and fecal samples will be collected at the start and end of the intervention to analyse for immunological biomarkers and gut microbiome.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in inflammatory cytokine profile after moderate probiotic beer consumption.
Time Frame: 5 weeks
|
Changes in inflammatory cytokine profile (IFNg, TNFa, IL-1b, IL-2, IL-4, IL-6, IL-10, IL-12) in blood samples of individuals after moderate probiotic beer consumption, in comparison to moderate normal beer consumption.
|
5 weeks
|
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Changes in gut microbiome profile after moderate probiotic beer consumption.
Time Frame: 5 weeks
|
Changes in gut microbiome profile from DNA sequencing in stool samples after moderate probiotic beer consumption, in comparison to moderate normal beer consumption.
|
5 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 27, 2021
Primary Completion (Actual)
February 18, 2022
Study Completion (Actual)
February 18, 2022
Study Registration Dates
First Submitted
May 24, 2022
First Submitted That Met QC Criteria
May 27, 2022
First Posted (Actual)
June 2, 2022
Study Record Updates
Last Update Posted (Actual)
June 2, 2022
Last Update Submitted That Met QC Criteria
May 27, 2022
Last Verified
May 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021/00196
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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