Irritable Bowel Syndrome Trial, Recruiting NCT05803980 Sponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCS Condition: Irritable Bowel Syndrome
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Irritable Bowel Syndrome Trial, Recruiting

NCT05803980
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 are able to understand and sign a consent form agreeing to take part
  • You are 18 years old or older
  • You have been diagnosed with diarrhoea-predominant or unclassified IBS (irritable bowel syndrome), based on a standard set of diagnostic guidelines called Rome IV criteria
  • You have had a colonoscopy within the last 5 years that showed no other bowel diseases

Who may not be able to join:

  • You have taken antibiotics or probiotics in the 8 weeks before the study start date
  • You have a chronic inflammatory bowel condition such as Crohn's disease, ulcerative colitis, indeterminate colitis, or eosinophilic gastroenteritis, or you have bowel cancer, coeliac disease, or diverticular disease
  • You have uncontrolled heart failure or a serious heart condition where your heart is pumping at a very low level (confirm with trial site)
  • You have severe breathing or respiratory problems
  • You have a serious mental health condition or are considered psychologically unstable by your doctor
  • You have a medical reason why you cannot safely have a fecal microbiota transplant (a procedure that carries risks similar to those of a colonoscopy)
  • You have previously had surgery on your digestive tract, unless it was only a gallbladder removal, appendix removal, or surgery that did not involve the digestive system
  • You have a stoma (an opening on your abdomen connected to your digestive system)
  • You are pregnant or breastfeeding
  • You are currently taking part in another clinical trial involving a treatment or intervention
  • You are considered unable or unlikely to follow the study procedures as required
  • You have any other health condition that the study doctors believe would make it unsafe or unsuitable for you to join

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 28 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
23 December 2021
Est. completion
23 September 2025

Where this trial is recruiting

🇮🇹 Italy

Primary endpoints

Improving IBS symptoms assessed with the IBS severity scoring system (IBS-SSS); Number and severity grade of adverse events after FMT

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: 28 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