Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Probiotic in IBS-D and functional diarrhea (three-month test)

Official title: Efficacy of Lactic Acid Bacteria in Managing Diarrhea-Associated Functional Gastrointestinal Disorders: A Randomized Controlled Trial

Run by Szeged University · NCT07916688 · Data updated 2026-11-12

A probiotic capsule is being tested to see if it can improve symptoms and quality of life for adults with diarrhea-predominant IBS or functional diarrhea compared with a placebo.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment100 (estimated)
SponsorSzeged University
Academic / other
Locations1 site (Szeged)
StatusRecruiting
StartedNovember 2026
Main results expectedNovember 2028
Study endsNovember 2029
Registry record updatedNovember 4, 2026
Trial IDNCT07916688 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 years or older with IBS-D or functional diarrhea diagnosed by Rome V criteria and stable on current IBS/FD treatment for at least 1 month.

Probably not a fit

Results may show no meaningful improvement for some individuals or may indicate limited benefit for others.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Adults with IBS-D or functional diarrhea will take a daily probiotic capsule for 3 months and then switch to a placebo for another 3 months, or vice versa, in a randomized, blinded design. Participants will complete quality-of-life questionnaires and track bowel habits to see if the probiotic helps normalize stool and reduce bowel movements. The study also aims to assess safety and tolerability of the probiotic. Rome V criteria are used to confirm eligibility, and prior stable treatment for IBS-D/FD is required.

Why it matters

Potential benefit: If successful, the probiotic could offer a safe way to improve symptoms and daily living for people with IBS-D or functional diarrhea.

How similar studies have gone: Previous research with probiotics has shown mixed results; this study builds on prior approaches but remains exploratory for this specific probiotic.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adults aged 18 years or older.
* Have diarrhea-predominant irritable bowel syndrome (IBS-D) or functional diarrhea (FD) diagnosed using Rome V criteria.
* Have had symptoms for at least 6 months.
* Have no warning signs that suggest another digestive disease.
* Have been taking the same treatment for IBS-D, FD, and other medical conditions for at least 1 month before joining the study.
* Are willing and able to provide written informed consent and follow study procedures.

Exclusion Criteria:

* Took antibiotics or probiotic products within the past 4 weeks.
* Had abdominal surgery in the past, except appendix removal (appendectomy).
* Have another type of irritable bowel syndrome or another functional digestive disorder.
* Have a known digestive disease that may explain their symptoms.
* Plan to start a new medication or change the dose of an existing medication during the study (except antispasmodic medications).
* Are unable or unwilling to complete study questionnaires and daily symptom records.

Where it's running

  • University of Szeged
    Szeged, Hungary
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.