RecruitingNot ApplicableNCT07235215

Vivatlac in Irritable Bowel Syndrome II (ViIBS2)

Effects of Vivatlac Synbiotic in Patients With Irritable Bowel Syndrome - A Randomized, Double-blind, Placebo-Controlled, 36 Weeks Clinical Trial


Sponsor

The President Stanisław Wojciechowski State University of Applied Sciences in Kalisz

Enrollment

200 participants

Start Date

Nov 21, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Multi-center,randomized, double-blind, placebo-controlled, 36 weeks trial investigating the effects of a nine-strain synbiotic (Vivatlac Synbiotikum) in IBS patients


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Inclusion Criteria2

  • diagnosed for Irritable Bowel Syndrome using the IBS questionnaire for Health Care Providers of the World Global Gastroenterology Organization
  • IBS-SSS ≥ 175 points

Exclusion Criteria9

  • patients currently taking products containing probiotics or have taken this kind of products during the last 3 months
  • patients currently taking antibiotics or have taken antibiotics during the last 3 months
  • patients having a concurrent severe illness (malignancies, uncontrolled hypertension or diabetes, hepatic, renal or cardiac dysfunctions, serious neurological disorders, psychosis, respiratory disorders such as asthma or COPD, hyper- or hypothyroidism
  • patients having chronic bowel disorders other than IBS, including inflammatory bowel disease, gastroenteritis, stomach and duodenal cancer, celiac disease
  • patient being pregnant, lactating, or planning to become pregnant during the next 9 months
  • patient being diagnosed to have a lactose intolerance
  • patients using motility drugs or dietary fiber supplements withing 2 weeks before study start
  • patient taking anti-coagulant medication
  • patients have participated in another clinical trial within the last three months

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Interventions

DIETARY_SUPPLEMENTVivatlac Synbiotic

Vivatlac Synbiotic containing a total of 4.5 x 10\^9 colony forming units (CFU) of nine different probiotic bacteria. Probiotic bacteria strains and their CFU amount per capsule are: Lactococcus lactis Ll-23, 9.00 x 10\^8 CFU; Lactobacillus helveticus SP 27, 9.00 x 10\^8 CFU; Bifidobacterium longum Bl-05, 6.75 x 10\^8 CFU; Bifidobacterium longum ES1, 4.50 x 10\^8 CFU; Lacticaseibacillus rhamnosus Lr-32, 4.50 x 10\^8 CFU; Streptococcus thermophiles St-21, 4.50 x 10\^8 CFU; Lacticaseibacillus casei Lc-11, 2.25 x 10\^8 CFU; Lactiplantibacillus plantarum Lp-115, 2.25 x 10\^8 CFU; Bifidobacterium bifidum Bb-02, 2.25 x 10\^8 CFU. As a prebiotic component each capsule contains 63 mg of fructooligosaccharides.

DIETARY_SUPPLEMENTPlacebo

Capsule containing maize starch with identical appearance as verum.


Locations(3)

District Hospital Jarocin

Jarocin, Poland

GP Clinic Spitalna

Jarocin, Poland

GP Clinic Wroclawska

Jarocin, Poland

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NCT07235215


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