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.
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
- Conditions the study is for
- Dementia; Alzheimer, Mixed Type (Etiology)
- 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.
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 group | Role | What they receive |
|---|---|---|
| Probiotic | Active comparator | Bifidobacterium 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 |
| Placebo | Placebo comparator | 3g 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.
Butyrate producing bacteria
abundance of butyrate producing bacteria
Measured: 6 months
Secondary outcomes (25)
Butyrate producing bacteria
abundance of butyrate producing bacteria
Measured: 12 months
diaminooxidase concentration in serum
marker of intestinal permeability
Measured: 6 months
diaminooxidase concentration in serum
marker of intestinal permeability
Measured: 12 months
zonulin concentration in stool
marker of intestinal permeability
Measured: 6 months
zonulin concentration in stool
marker of intestinal permeability
Measured: 12 months
calprotectin concentration in stool
marker of intestinal inflammation
Measured: 6 months
calprotectin concentration in stool
marker of intestinal inflammation
Measured: 12 months
soluble CD 14 concentration in serum
marker of systemic inflammation
Measured: 6 months
soluble CD 14 concentration in serum
marker of systemic inflammation
Measured: 12 months
lipopolysaccharide binding protein concentration in serum
marker of systemic inflammation
Measured: 6 months
lipopolysaccharide binding protein concentration in serum
marker of systemic inflammation
Measured: 12 months
lipopolysaccharide concentration in serum
marker of bacterial translocation
Measured: 6 months
lipopolysaccharide concentration in serum
marker of bacterial translocation
Measured: 12 months
peptidoglycan concentration in serum
marker of bacterial translocation
Measured: 6 months
peptidoglycan concentration in serum
marker of bacterial translocation
Measured: 12 months
bacterial DNA concentration in serum
marker of bacterial translocation
Measured: 6 months
bacterial DNA concentration in serum
marker of bacterial translocation
Measured: 12 months
Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS cog)
Questionnaire to assess cognitive function, 0-70 points
Measured: 6 months
Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS cog)
Questionnaire to assess cognitive function, 0-70 points
Measured: 12 months
Mini mental state examination
Questionnaire to assess cognitive function, 0-30 points
Measured: 6 months
Mini mental state examination
Questionnaire to assess cognitive function, 0-30 points
Measured: 12 months
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
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
Barthel index
Assessment of activities of daily living, 0-100 points
Measured: 6 months
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.
- First posted20 Feb 2019
- Study start15 Jun 2019
- Primary completion31 Dec 2024
- Study completion31 Dec 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Dementia; Alzheimer, Mixed Type (Etiology)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Medical University of Graz
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
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
Study at a glance
From the registry record, last updated by the sponsor on 12 Feb 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Probiotics in Dementia
- ClinicalTrials.gov ID
- NCT03847714
- Acronym / sponsor ID
- PIDE / PIDE
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 17 participants (actual)
- Lead sponsor
- Medical University of GrazUniversity, hospital or other
- Study start
- 15 Jun 2019 (actual)
- Primary completion
- 31 Dec 2024 (actual)
- Study completion
- 31 Dec 2024 (actual)
- First posted
- 20 Feb 2019 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Probiotic | Active comparator | Dietary Supplement: Omni-Biotic Stress RepairBifidobacterium 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 |
| Placebo | Placebo comparator | Dietary Supplement: placebo3g of a similar looking and tasting powder, twice daily |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- 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
Key exclusion criteria (8 listed)
- Other forms of dementia
- Inflammatory bowel diseases
- Liver cirrhosis
- Antibiotic treatment within the last 4 weeks
- Febrile illness within the last 4 weeks
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Omni-Biotic Stress RepairAlso: Omni-Biotic SR-9, Winclove 825The 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). | Dietary supplement | Probiotic |
| placebosimilar looking and tasting powder | Dietary supplement | Placebo |
Primary outcome
Butyrate producing bacteria
Time frame: 6 months
abundance of butyrate producing bacteria
25 secondary outcomes
Butyrate producing bacteria
Time frame: 12 months
diaminooxidase concentration in serum
Time frame: 6 months
diaminooxidase concentration in serum
Time frame: 12 months
zonulin concentration in stool
Time frame: 6 months
zonulin concentration in stool
Time frame: 12 months
calprotectin concentration in stool
Time frame: 6 months
calprotectin concentration in stool
Time frame: 12 months
soluble CD 14 concentration in serum
Time frame: 6 months
soluble CD 14 concentration in serum
Time frame: 12 months
lipopolysaccharide binding protein concentration in serum
Time frame: 6 months
lipopolysaccharide binding protein concentration in serum
Time frame: 12 months
lipopolysaccharide concentration in serum
Time frame: 6 months
lipopolysaccharide concentration in serum
Time frame: 12 months
peptidoglycan concentration in serum
Time frame: 6 months
peptidoglycan concentration in serum
Time frame: 12 months
bacterial DNA concentration in serum
Time frame: 6 months
bacterial DNA concentration in serum
Time frame: 12 months
Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS cog)
Time frame: 6 months
Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS cog)
Time frame: 12 months
Mini mental state examination
Time frame: 6 months
Mini mental state examination
Time frame: 12 months
clinician's interview-based impression of change with caregiver input (CIBIC+)
Time frame: 6 months
clinician's interview-based impression of change with caregiver input (CIBIC+)
Time frame: 12 months
Barthel index
Time frame: 6 months
Barthel index
Time frame: 12 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Feb 2025.
- Individual participant dataSharing planned: Yes. microbiome sequencing data will be published at nucleotide archive
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
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.