Irritable Bowel Syndrome Trial, Recruiting NCT07235215 Sponsor: The President Stanisław Wojciechowski State University of Applied Sciences in Kalisz Condition: Irritable Bowel Syndrome
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Irritable Bowel Syndrome Trial, Recruiting

NCT07235215
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You have been diagnosed with Irritable Bowel Syndrome (IBS) using a specific questionnaire from the World Global Gastroenterology Organization
  • Your IBS symptoms are rated at 175 points or higher on a standard IBS symptom severity scoring system (confirm with trial site)

Who may not be able to join:

  • You are currently taking probiotic products (such as certain yogurts, supplements, or drinks with live cultures), or have taken them in the last 3 months
  • You are currently taking antibiotics, or have taken them in the last 3 months
  • You have another serious illness, such as cancer, poorly controlled high blood pressure or diabetes, liver, kidney or heart problems, serious neurological or mental health conditions, breathing conditions like asthma or COPD, or a thyroid disorder
  • You have a chronic bowel condition other than IBS, such as inflammatory bowel disease, gastroenteritis, stomach or bowel cancer, or coeliac disease
  • You are pregnant, breastfeeding, or planning to become pregnant in the next 9 months
  • You have been diagnosed with lactose intolerance
  • You have used medication to help with gut movement or fibre supplements within 2 weeks before the trial starts
  • You are taking blood-thinning (anti-coagulant) medication
  • You have taken part in another clinical trial within the last 3 months

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Jacek Piatek, Prof. Dr., The President Stanisław Wojciechowski State University of Applied Sciences in Kalisz

Phone: +48883389788

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
The President Stanisław Wojciechowski State University of Applied Sciences in Kalisz
Registry
ClinicalTrials.gov
Start date
21 November 2025
Est. completion
1 December 2026

Where this trial is recruiting

🇵🇱 Poland

Primary endpoints

Severity of IBS using the IBS-Severity Scoring System (IBS-SSS); Changes of IBS severity using the IBS Global Improvement Scale (IBS-GIS); Changes in adequate relief of IBS-symptoms (IBS-AR)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov