Vivatlac in Irritable Bowel Syndrome II (ViIBS2)
Recruiting now · Not applicable · Has a placebo group
Conditions studied: Irritable Bowel Syndrome
In brief
Multi-center,randomized, double-blind, placebo-controlled, 36 weeks trial investigating the effects of a nine-strain synbiotic (Vivatlac Synbiotikum) in IBS patients
Key facts
- Study ID
- NCT07235215
- Run by
- The President Stanisław Wojciechowski State University of Applied Sciences in Kalisz
- People needed
- 200
- Starts
- 2025-11-21
- Expected to finish
- 2027-12-01
- Last updated by the study team
- 2025-12-15
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- diagnosed for Irritable Bowel Syndrome using the IBS questionnaire for Health Care Providers of the World Global Gastroenterology Organization
- IBS-SSS ≥ 175 points
You may not qualify if…
- 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
Where it is running
- District Hospital Jarocin — Jarocin, Poland (enrolling)
- GP Clinic Spitalna — Jarocin, Poland (enrolling)
- GP Clinic Wroclawska — Jarocin, Poland (enrolling)
Full record on ClinicalTrials.gov
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