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Dementia; Alzheimer, Mixed Type (Etiology)PIDENCT03847714

Probiotics in Dementia

A study testing Omni-Biotic Stress Repair in people with Dementia; Alzheimer, Mixed Type (Etiology), run by Medical University of Graz at 1 site in Austria.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Dementia is associated with changes in gut microbiome composition, gut barrier dysfunction, intestinal inflammation and systemic inflammation. Probiotics are a possibility to modulate the gut-brain axis. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Omni-Biotic Stress Repair
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
17 participants
Where
1 siteAustria
Study dates
15 Jun 2019to 31 Dec 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age >18 years
  • Dementia of Alzheimer type and mixed type (diagnosis by a board-certified neurologist/psychiatrist and according to ICD10)
  • Mini Mental State Examination 21-26
  • Stable treatment with anti-dementia drugs including phytotherapeutics (>3 months) or no intention to start anti-dementia drugs
  • Informed consent

Who cannot join

  • Other forms of dementia
  • Inflammatory bowel diseases
  • Liver cirrhosis
  • Antibiotic treatment within the last 4 weeks
  • Febrile illness within the last 4 weeks
  • Acute hospital admission for dementia-unrelated reasons within the last 4 weeks
  • Dysphagia
  • Any other condition or circumstance, which, in the opinion of the investigator, would affect the patient's ability to participate in the protocol

Trial locations and contacts

1 site in 1 country.

Austria1 site
  • Medical University Graz

    Graz

Other trials in Austria

About this study

Dementia is associated with changes in gut microbiome composition, gut barrier dysfunction, intestinal inflammation and systemic inflammation. Probiotics are a possibility to modulate the gut-brain axis. In this study the effect of probiotics on the gut microbiome and, gut barrier function, inflammation and cognitive dysfunction will be studied.

Read the detailed description

Dementia is a disease that presents with deterioration in memory, thinking, behaviour and the ability to perform everyday activities. Worldwide 47.5 million people are affected and incidence of dementia is increasing. Dementia leads to disability and dependency among older people worldwide and thereby has a huge physical, psychological, social and economic impact on caregivers, families and society. Alzheimer's disease (AD) is the most common form of dementia accounting for 60-70% of the cases; other forms include Lewy body dementia, frontotemporal dementia, vascular dementia and Parkinson's disease with dementia. In AD, pathologic protein aggregates of amyloid beta and hyperphosphorylated tangles of tau-protein which deposit as neurofibrillary tangles are typical features. This leads to neuroinflammation, mainly mediated by the innate immune system. The most important cells in this process are microglia cells, which represent the resident macrophages of the brain. Although microglia is able to remove extracellular amyloid beta, in later stages of the disease cells remain in a dystrophic state and cannot exert their beneficial functions. Microglia maturation and function is critically dependent on short-chain fatty acids produced by the gut microbiome and therefore highlights the microbiome as a potential diagnostic and therapeutic target in dementia.

The role of the commensal microbial population of the human body - especially the intestinal microbiome - in various diseases is emerging due to the development of advanced analysis techniques. Recently the concept of the gut brain-axis has been established. Several pathways including the autonomic nervous system, the enteric nervous system, the neuroendocrine system and the immune system allow a communication between gut and brain but may also be involved in disease development.

During ageing, the gut microbiome composition undergoes changes. A decrease in diversity, a loss of beneficial taxa and an increase of facultative pathogens has been described. Diet and the place of residence play an important role in the shaping of the microbiome. Aging is also associated with inflammation - often termed as "inflammaging" associated with an increase in gut permeability, mucosal inflammation and bacterial translocation.

Since the main risk factor for developing dementia, especially AD, is aging, it is very likely that the gut-brain axis is critically involved in dementia development.

Animal studies so far suggest that AD is associated with changes in the gut microbiome composition with a decrease in beneficial, anti-inflammatory genera. Furthermore, genetic alterations in amyloid genes can influence microbiome composition in mice, pointing towards a vicious cycle in AD development.

In humans, so far only limited evidence on the microbiome composition in patients with dementia is available. There is evidence that the composition of the microbiome in subgingival plaques is altered in dementia and associated with cognitive function. Recently the first human study identified phylum- through genus-wide differences in bacterial abundance including decreased Firmicutes, increased Bacteroidetes, and decreased Bifidobacterium in the stool of AD patients.

Being tested
Omni-Biotic Stress Repair, placebo
Medical subject headings
Dementia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Omni-Biotic Stress RepairDietary supplement

    Also called Omni-Biotic SR-9, Winclove 825

    The probiotic supplement is a commercially available food for special medical purposes and includes 9 bacterial strains with at least 7.5 billion organisms (7.5 × 109 Colony Forming Units/g) per 1 portion (= 3 g).

  • placeboDietary supplement

    similar looking and tasting powder

Study groups in NCT03847714
Study groupRoleWhat they receive
ProbioticActive comparatorBifidobacterium bifidum W23, B. lactis W51, B. lactis W52, Lactobacillus acidophilus W22, L. casei W56, L. paracasei W20, L. plantarum W62, L. salivarius W24, Lactococcus lactis W19, 7.5 × 109 Colony Forming Units/g twice daily dissolved in water
Receives: Dietary Supplement: Omni-Biotic Stress Repair
PlaceboPlacebo comparator3g of a similar looking and tasting powder, twice daily
Receives: Dietary Supplement: placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Butyrate producing bacteria

    abundance of butyrate producing bacteria

    Measured: 6 months

Secondary outcomes (25)
  1. Butyrate producing bacteria

    abundance of butyrate producing bacteria

    Measured: 12 months

  2. diaminooxidase concentration in serum

    marker of intestinal permeability

    Measured: 6 months

  3. diaminooxidase concentration in serum

    marker of intestinal permeability

    Measured: 12 months

  4. zonulin concentration in stool

    marker of intestinal permeability

    Measured: 6 months

  5. zonulin concentration in stool

    marker of intestinal permeability

    Measured: 12 months

  6. calprotectin concentration in stool

    marker of intestinal inflammation

    Measured: 6 months

  7. calprotectin concentration in stool

    marker of intestinal inflammation

    Measured: 12 months

  8. soluble CD 14 concentration in serum

    marker of systemic inflammation

    Measured: 6 months

  9. soluble CD 14 concentration in serum

    marker of systemic inflammation

    Measured: 12 months

  10. lipopolysaccharide binding protein concentration in serum

    marker of systemic inflammation

    Measured: 6 months

  11. lipopolysaccharide binding protein concentration in serum

    marker of systemic inflammation

    Measured: 12 months

  12. lipopolysaccharide concentration in serum

    marker of bacterial translocation

    Measured: 6 months

  13. lipopolysaccharide concentration in serum

    marker of bacterial translocation

    Measured: 12 months

  14. peptidoglycan concentration in serum

    marker of bacterial translocation

    Measured: 6 months

  15. peptidoglycan concentration in serum

    marker of bacterial translocation

    Measured: 12 months

  16. bacterial DNA concentration in serum

    marker of bacterial translocation

    Measured: 6 months

  17. bacterial DNA concentration in serum

    marker of bacterial translocation

    Measured: 12 months

  18. Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS cog)

    Questionnaire to assess cognitive function, 0-70 points

    Measured: 6 months

  19. Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS cog)

    Questionnaire to assess cognitive function, 0-70 points

    Measured: 12 months

  20. Mini mental state examination

    Questionnaire to assess cognitive function, 0-30 points

    Measured: 6 months

  21. Mini mental state examination

    Questionnaire to assess cognitive function, 0-30 points

    Measured: 12 months

  22. clinician's interview-based impression of change with caregiver input (CIBIC+)

    Questionnaire to assess overall change during the study, 1-7 points

    Measured: 6 months

  23. clinician's interview-based impression of change with caregiver input (CIBIC+)

    Questionnaire to assess overall change during the study, 1-7 points

    Measured: 12 months

  24. Barthel index

    Assessment of activities of daily living, 0-100 points

    Measured: 6 months

  25. Barthel index

    Assessment of activities of daily living, 0-100 points

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Feb 2019
  2. Study start15 Jun 2019
  3. Primary completion31 Dec 2024
  4. Study completion31 Dec 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
17 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03847714
Sponsor's protocol ID
PIDE
Acronym
PIDE
Status last verified
Mar 2024
First submitted
11 Feb 2019
Last updated
12 Feb 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: microbiome sequencing data will be published at nucleotide archive

Questions about this trial

What is this clinical trial studying?

A study testing Omni-Biotic Stress Repair in people with Dementia; Alzheimer, Mixed Type (Etiology), run by Medical University of Graz at 1 site in Austria.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 12 Feb 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Austria. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Butyrate producing bacteria (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Feb 2025; AzTrials last refreshed its copy on 28 Oct 2026.

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