Crohn DiseaseNCT01765439
The Effect of VSL#3 Probiotic Preparation on the Bile Acid Metabolism in Patients With Inflammatory Bowel Disease
A study testing VSL#3 (Original De Simone formulation) in people with Crohn Disease and Ulcerative Colitis, run by Charles University, Czech Republic at 1 site in Czechia.
Trial summary
The aim of the study is to determine, whether administration of VSL#3 (Original De Simone formulation) probiotic preparation can alter the bile acid metabolism in patients with inflammatory bowel disease. Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Crohn Disease, Ulcerative Colitis
- What is being tested?
- VSL#3 (Original De Simone formulation)
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 79 participants
- Where
- 1 siteCzechia
- Study dates
- Feb 2014to Dec 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Who may be able to join
- Arm CD resected
- confirmed diagnosis of Crohn´s disease (at least 6 months)
- history of single resection of terminal ileum (at least 6 months before inclusion)
- maximum length of resected ileum is 60 cm
- no signs of disease activity (clinical, endoscopical, laboratory)
- stable medication
Show all 18Show fewer
- Arm UC unoperated
- confirmed diagnosis of ulcerative colitis (at least 6 months)
- no signs of disease activity (clinical, endoscopical, laboratory)
- stable medication
- Arm UC IPAA
- confirmed diagnosis of ulcerative colitis (at least 6 months)
- proctocolectomy and IPAA (at least 3 months before inclusion)
- no signs of disease activity (clinical, endoscopical, laboratory)
- stable medication
- Arm Healthy volunteers
- no signs of gastrointestinal disorder
- initial laboratory examination within normal range (blood count, liver function tests, C-reactive protein, Fe, ferritin, fecal calprotectin)
Who cannot join
- use of bile acids
- use of bile acids sequestrants
- use of farnesoid X receptor agonists/antagonists
- recent colonoscopy(less than 1 month before inclusion)
- diabetes
Trial locations and contacts
1 site in 1 country.
About this study
Official title: The Effect of VSL#3 (Original De Simone Formulation) Probiotic Preparation on the Bile Acid Metabolism in Patients With Inflammatory Bowel Disease
The aim of the study is to determine, whether administration of VSL#3 (Original De Simone formulation) probiotic preparation can alter the bile acid metabolism in patients with inflammatory bowel disease.
Read the detailed description
VSL#3 (Original De Simone formulation, further abbreviated as VSL#3), a potent probiotic preparation, has been tested as an adjuvant therapy in inflammatory bowel diseases (IBD), chronic unspecific inflammatory disorders of the gastrointestinal tract (the most frequent forms of IBD are Crohn's disease (CD) and ulcerative colitis (UC)). VSL#3 has been shown to improve symptoms of IBD both in animal models and in humans-the most impressive results have been observed in preventing of pouchitis in UC patients. Several possible mechanisms of its action have been suggested, including change in gut microbial diversity, immunomodulatory function (upregulation of interleukine-10), etc., however, the list is probably far from complete.
Bile acids (BA) play an important role in the gastrointestinal tract - besides facilitating fat (and protein) digestion and resorption, they act as general antimicrobial agents within the small intestine (maintaining the small intestine more or less microbe-free), colonic microflora modifiers, intestinal innate immunity regulators, and importantly as signalling molecules on the liver-intestine/intestine-liver axis. Under pathological conditions (such as BA malabsorption) BA can worsen the IBD symptoms (namely diarrhoea), by irritating colonic mucosa or by inducing colonic secretion of electrolytes.
The study hypothesis is that the beneficial effect of VSL#3 might be partially explained by alteration of BA metabolism. There exists a complex crosstalk between gut microflora and BA: BA affect microbial growth, whereas BA structure is modified by bacteria (deconjugation, 7 α dehydroxylation). Several observations might support this hypothesis: VSL#3 ameliorates symptoms of radiation or chemotherapy induced diarrhoea, as well as diarrhoea of critically ill patients - conditions, that can be caused by BA malabsorption. Similarly, oxalate absorption (closely related to BA malabsorption) has been shown to be lowered by VSL#3. The main question to be addressed in the proposed study is, therefore, whether VSL#3 administration can somehow change metabolism of bile acids (BA).
Additionally, urinary metabolite levels are strongly influenced by differences in the intestinal microbiota, since both gut bacterial metabolism, and shared metabolism by the host and bacterial species ('co-metabolism'), generate specific metabolic products. Such metabolites may therefore be used as markers of microbial metabolic activity, reflecting systemic, functional differences. This application of urinary metabolic profiling avoids the technical difficulties, and methodological differences, found in molecular studies of the intestinal microbiota in IBD, which have contributed to often discrepant findings. Specific urinary metabolites related to gut microbial metabolism differ between CD patients, UC patients, and controls. The emerging technique of urinary NMR-based metabolic profiling with multivariate analysis was able to distinguish these cohorts. This study should address the question, whether VSL#3 administration changes the nuclear magnetic resonance-based urinary metabolomic profile.
- Conditions
- Crohn Disease, Ulcerative Colitis
- Being tested
- VSL#3 (Original De Simone formulation)
- Keywords
- bile acids, metabolism, probiotics
- Medical subject headings
- Crohn Disease, Colitis, Ulcerative
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
VSL#3 (Original De Simone formulation)Dietary supplement
Study subjects will receive two sachets of VSL#3 probiotic (ie 2x900 billions of live bacteria) per day (one in the morning, one in the evening). The intervention period will be 6 weeks (plus or minus 5 days).
| Study group | Role | What they receive |
|---|---|---|
| CD resected | Experimental | Patients with Crohn´s disease with the history of single resection (<60 cm) of distal leum. Receives: Dietary Supplement: VSL#3 (Original De Simone formulation) |
| UC unoperated | Experimental | Patients with ulcerative colitis without history of gut resection. Receives: Dietary Supplement: VSL#3 (Original De Simone formulation) |
| UC IPAA | Experimental | Patients with ulcerative colitis after proctocolectomy and ileal pouch-anal anastomosis(IPAA). Receives: Dietary Supplement: VSL#3 (Original De Simone formulation) |
| Healthy volunteers | Experimental | Subjects without any sign of disease of the digestive tract. Receives: Dietary Supplement: VSL#3 (Original De Simone formulation) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Alteration in the rate of bile acid synthesis
Will be assessed as difference between serum levels of fibroblast growth factor 19 and C4 at baseline and 6 weeks, respectively.
Measured: Baseline and 6 weeks (plus or minus 5 days)
Secondary outcomes (2)
Change of the spectrum of bile acids in stools and plasma
Measured: Baseline and 6 weeks (plus or minus 5 days).
Change of a metabolomic profile in urine
Measured: Baseline and 6 weeks (plus or minus 5 days).
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Jan 2013 (estimated)
- Study startFeb 2014
- Primary completionAug 2027 (estimated)
- Study completionDec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Crohn DiseaseStudies of the same condition, open and under way.
- More trials run by Charles University, Czech RepublicThe sponsor's other registered studies.
- 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
- Basic science
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 79 participants (actual)
Sponsor and investigators
- Lead sponsor
- Charles University, Czech Republic
- Sponsor type
- University, hospital or other
- Collaborators
- Iscare i.v.f., Czech Republic, CD Investments srl, University Of Perugia, University of Roma La Sapienza
- Responsible party
- Principal investigator, Martin Lenicek, Charles University, Czech Republic
- Investigators
- Martin Lenicek, MD, Ph.D., Principal investigator, Charles University, Czech Republic
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01765439
- Sponsor's protocol ID
- VSL#3-2013-CR
- Status last verified
- Apr 2026
- First submitted
- 7 Jan 2013
- Last updated
- 23 Apr 2026
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 23 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of VSL#3 (Original De Simone Formulation) Probiotic Preparation on the Bile Acid Metabolism in Patients With Inflammatory Bowel Disease
- ClinicalTrials.gov ID
- NCT01765439
- Acronym / sponsor ID
- VSL#3-2013-CR
- Conditions
- Crohn Disease, Ulcerative Colitis
- Keywords
- bile acids, metabolism, probiotics
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 79 participants (actual)
- Lead sponsor
- Charles University, Czech RepublicUniversity, hospital or other
- Collaborators
- Iscare i.v.f., Czech Republic, CD Investments srl, University Of Perugia, University of Roma La Sapienza
- Study start
- Feb 2014
- Primary completion
- Aug 2027 (estimated)
- Study completion
- Dec 2027 (estimated)
- First posted
- 10 Jan 2013 (estimated)
- 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.
The aim of the study is to determine, whether administration of VSL#3 (Original De Simone formulation) probiotic preparation can alter the bile acid metabolism in patients with inflammatory bowel disease.
Detailed description
VSL#3 (Original De Simone formulation, further abbreviated as VSL#3), a potent probiotic preparation, has been tested as an adjuvant therapy in inflammatory bowel diseases (IBD), chronic unspecific inflammatory disorders of the gastrointestinal tract (the most frequent forms of IBD are Crohn's disease (CD) and ulcerative colitis (UC)). VSL#3 has been shown to improve symptoms of IBD both in animal models and in humans-the most impressive results have been observed in preventing of pouchitis in UC patients. Several possible mechanisms of its action have been suggested, including change in gut microbial diversity, immunomodulatory function (upregulation of interleukine-10), etc., however, the list is probably far from complete.
Bile acids (BA) play an important role in the gastrointestinal tract - besides facilitating fat (and protein) digestion and resorption, they act as general antimicrobial agents within the small intestine (maintaining the small intestine more or less microbe-free), colonic microflora modifiers, intestinal innate immunity regulators, and importantly as signalling molecules on the liver-intestine/intestine-liver axis. Under pathological conditions (such as BA malabsorption) BA can worsen the IBD symptoms (namely diarrhoea), by irritating colonic mucosa or by inducing colonic secretion of electrolytes.
The study hypothesis is that the beneficial effect of VSL#3 might be partially explained by alteration of BA metabolism. There exists a complex crosstalk between gut microflora and BA: BA affect microbial growth, whereas BA structure is modified by bacteria (deconjugation, 7 α dehydroxylation). Several observations might support this hypothesis: VSL#3 ameliorates symptoms of radiation or chemotherapy induced diarrhoea, as well as diarrhoea of critically ill patients - conditions, that can be caused by BA malabsorption. Similarly, oxalate absorption (closely related to BA malabsorption) has been shown to be lowered by VSL#3. The main question to be addressed in the proposed study is, therefore, whether VSL#3 administration can somehow change metabolism of bile acids (BA).
Additionally, urinary metabolite levels are strongly influenced by differences in the intestinal microbiota, since both gut bacterial metabolism, and shared metabolism by the host and bacterial species ('co-metabolism'), generate specific metabolic products. Such metabolites may therefore be used as markers of microbial metabolic activity, reflecting systemic, functional differences. This application of urinary metabolic profiling avoids the technical difficulties, and methodological differences, found in molecular studies of the intestinal microbiota in IBD, which have contributed to often discrepant findings. Specific urinary metabolites related to gut microbial metabolism differ between CD patients, UC patients, and controls. The emerging technique of urinary NMR-based metabolic profiling with multivariate analysis was able to distinguish these cohorts. This study should address the question, whether VSL#3 administration changes the nuclear magnetic resonance-based urinary metabolomic profile.
Study design
- Primary purpose
- Basic science
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| CD resected | Experimental | Dietary Supplement: VSL#3 (Original De Simone formulation)Patients with Crohn´s disease with the history of single resection (<60 cm) of distal leum. |
| UC unoperated | Experimental | Dietary Supplement: VSL#3 (Original De Simone formulation)Patients with ulcerative colitis without history of gut resection. |
| UC IPAA | Experimental | Dietary Supplement: VSL#3 (Original De Simone formulation)Patients with ulcerative colitis after proctocolectomy and ileal pouch-anal anastomosis(IPAA). |
| Healthy volunteers | Experimental | Dietary Supplement: VSL#3 (Original De Simone formulation)Subjects without any sign of disease of the digestive tract. |
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (18 listed)
- Arm CD resected
- confirmed diagnosis of Crohn´s disease (at least 6 months)
- history of single resection of terminal ileum (at least 6 months before inclusion)
- maximum length of resected ileum is 60 cm
- no signs of disease activity (clinical, endoscopical, laboratory)
Key exclusion criteria (5 listed)
- use of bile acids
- use of bile acids sequestrants
- use of farnesoid X receptor agonists/antagonists
- recent colonoscopy(less than 1 month before inclusion)
- diabetes
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 |
|---|---|---|
| VSL#3 (Original De Simone formulation)Study subjects will receive two sachets of VSL#3 probiotic (ie 2x900 billions of live bacteria) per day (one in the morning, one in the evening). The intervention period will be 6 weeks (plus or minus 5 days). | Dietary supplement | CD resected, Healthy volunteers, UC IPAA, UC unoperated |
Primary outcome
Alteration in the rate of bile acid synthesis
Time frame: Baseline and 6 weeks (plus or minus 5 days)
Will be assessed as difference between serum levels of fibroblast growth factor 19 and C4 at baseline and 6 weeks, respectively.
2 secondary outcomes
Change of the spectrum of bile acids in stools and plasma
Time frame: Baseline and 6 weeks (plus or minus 5 days).
Change of a metabolomic profile in urine
Time frame: Baseline and 6 weeks (plus or minus 5 days).
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Apr 2026.
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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.
Martin Lenicek, MD, Ph.D. principal investigator
Charles University, Czech Republic
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing VSL#3 (Original De Simone formulation) in people with Crohn Disease and Ulcerative Colitis, run by Charles University, Czech Republic at 1 site in Czechia.
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 18 inclusion and 5 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: under way, not looking for participants, as of the sponsor's last update on 23 Apr 2026. 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 Czechia. 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. 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?
This study is still under way. Results are not available in the source record yet.
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?
Alteration in the rate of bile acid synthesis (time frame: Baseline and 6 weeks (plus or minus 5 days)). 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 23 Apr 2026.