Clinical trial No longer in our active list Interventional

Probiotics improving intestinal barrier function

Official title: Effects of DL-endopeptidase Produced by Probiotics on Human Intestinal NOD2 Ligands and Related Functions

Run by Zhujiang Hospital · NCT06716047 · Data updated 2026-05-14

This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.

This study is testing whether a special probiotic can help improve gut health by repairing the intestinal barrier in people with digestive issues.

Quick facts

Study typeInterventional
SexAll
Enrollment80 (estimated)
SponsorZhujiang Hospital
Academic / other
Locations1 site (Canton, Guangzhou)
Trial IDNCT06716047 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are individuals interested in improving their gut health and who meet the inclusion criteria.

Probably not a fit

Patients with severe digestive symptoms or chronic diseases may not benefit from this study.

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

What this trial studies

This trial investigates the effects of a specific probiotic that produces DL-endopeptidase on human intestinal health. Participants will take the probiotic orally for a designated period, during which blood and stool samples will be collected, along with questionnaires to assess efficacy and safety. The study aims to evaluate how this probiotic can repair the intestinal barrier and regulate enteritis, contributing to overall gut health.

Why it matters

Potential benefit: If successful, this could enhance gut health and improve intestinal barrier function for patients.

How similar studies have gone: Other studies have shown promising results with probiotics in gut health, suggesting potential success for this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* tend to participate the trial

Exclusion Criteria:

* severe digestive symptoms, such as severe vomiting, hematochezia, bloody or tarry stool within one month before intervention; antibiotics or laxatives or probiotics or intestinal antiulcer agent within one month before intervention; previous or current treatment for any diseases or illnesses such as gastrointestinal disease (gastric ulcers, Crohn's, celiac, ulcerative colitis, etc.); other chronic diseases (diabetes, kidney disease, etc.) or immunecompromising diseases or conditions (HIV/AIDS, autoimmune, hepatitis, cancer, transplant patient etc.); pregnant or lactating.

Where it's running

  • Industrial Avenue 253, canton
    Canton, Guangzhou, China
    Recruiting

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.
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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.