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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.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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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.

Czechia1 site
  • Iscare I.V.F.

    Prague, 17004

Other trials in Czechia

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.

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 groups in NCT01765439
Study groupRoleWhat they receive
CD resectedExperimentalPatients 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 unoperatedExperimentalPatients with ulcerative colitis without history of gut resection.
Receives: Dietary Supplement: VSL#3 (Original De Simone formulation)
UC IPAAExperimentalPatients with ulcerative colitis after proctocolectomy and ileal pouch-anal anastomosis(IPAA).
Receives: Dietary Supplement: VSL#3 (Original De Simone formulation)
Healthy volunteersExperimentalSubjects 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.

  1. 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)
  1. Change of the spectrum of bile acids in stools and plasma

    Measured: Baseline and 6 weeks (plus or minus 5 days).

  2. 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.

  1. First posted10 Jan 2013 (estimated)
  2. Study startFeb 2014
  3. Primary completionAug 2027 (estimated)
  4. Study completionDec 2027 (estimated)

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
Basic science
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
79 participants (actual)
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

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.

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