Sodium Butyrate and Kluyveromyces Marxianus Supplementation in Inflammatory Bowel Disease (Butymixx)
Safety and Tolerability of Sodium Butyrate and Kluyveromyces Marxianus Supplementation in Inflammatory Bowel Disease Treatment
The goal of this clinical trial is to learn if a dietary supplement called ButyMixx can help people with ulcerative colitis in remission feel better and keep their intestines less inflamed.
ButyMixx contains:
- Sodium butyrate, a substance normally produced by our gut microbiota that helps protect the intestinal lining and reduce inflammation.
- A "beneficial" yeast (Kluyveromyces marxianus), similar to probiotics, which may support the balance of the intestinal microbiota.
It will also learn about the safety of dietary supplement. The main questions it aims to answer are:
Does ButyMixx after 2 months of supplementation
- Symptoms improve,
- Quality of life improves,
- Intestinal inflammation decreases ,
- The gut microbiota becomes more "balanced"
- What medical problems do participants have when taking ButyMixx ?
Participants will:
- Take 2 sachets of ButyMixx per day for 8 weeks
Before starting and at the end of the 8 weeks:
- Provide a stool sample
- Complete a quality-of-life questionnaire
- Be assessed by a doctor using a symptom score
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
ButyMixx Study A novel natural supportive strategy for Ulcerative Colitis in remission What is ulcerative colitis? Ulcerative colitis (UC) is a chronic inflammatory bowel disease characterized by recurrent inflammation of the colonic mucosa, leading to symptoms such as diarrhea, rectal bleeding, abdominal pain, and fatigue.
Even during clinical remission, when symptoms are minimal or absent, the intestinal mucosa often remains fragile and susceptible to new inflammatory flares.
For this reason, current research is increasingly focused not only on treating acute disease activity, but also on identifying strategies able to maintain mucosal health over time, improve quality of life, and reduce the risk of relapse.
The role of the gut microbiota
The human gut hosts a complex community of microorganisms, known as the gut microbiota, which plays a crucial role in:
- digestion and nutrient metabolism
- protection against pathogenic microorganisms
- regulation of immune responses
- maintenance of intestinal barrier integrity In patients with UC, this microbial ecosystem is frequently altered (a condition known as dysbiosis), even during remission. Restoring a balanced microbiota is therefore considered a key therapeutic target.
What is ButyMixx?
ButyMixx is a dietary supplement combining two natural components:
Sodium butyrate
Butyrate is a short-chain fatty acid normally produced by bacterial fermentation of dietary fibers. It has several well-documented physiological functions:
- it is the main energy source for colonocytes
- supports epithelial repair and regeneration
- exerts anti-inflammatory effects
- contributes to the maintenance of intestinal barrier integrity In patients with UC, endogenous butyrate production is often reduced.
- Kluyveromyces marxianus
This is a probiotic yeast, commonly found in kefir, whose probiotic potential has been investigated in preclinical models. Studies have shown that K. marxianus:
- survives gastrointestinal transit efficiently
- interacts with the host immune system
- reduces pro-inflammatory signaling
- supports a more balanced intestinal microbiota It is recognized as safe by both European and US regulatory authorities.
Rationale of the study
The study was designed to investigate whether the combination of butyrate and probiotic yeast may represent a natural adjunctive strategy to standard pharmacological therapy (e.g., mesalamine and/or biologics), with the aim of:
- maintaining lower levels of intestinal inflammation
- improving patients' quality of life
- supporting gut microbiota homeostasis
- potentially reducing the risk of disease relapse
Study population
A total of 40 patients will be enrolled, meeting the following criteria:
- age between 18 and 75 years
- diagnosis of ulcerative colitis in clinical remission
- stable background medical therapy Patients with active disease, other forms of colitis, ongoing intestinal infections, pregnancy, or recent use of antibiotics/probiotics will be excluded.
Study design and procedures Study duration
- 8 weeks Supplement administration
- Two sachets of ButyMixx daily, taken before meals Study visits
Two visits are scheduled:
Baseline visit (T0)
- Clinical symptom assessment
- Quality-of-life questionnaire administration
Stool sample collection for:
- fecal calprotectin (marker of intestinal inflammation)
- gut microbiota analysis End-of-treatment visit (T1, after 8 weeks)
- Reassessment of symptoms and quality of life
- Repeat stool sample collection
- Recording of any adverse events
Study outcomes
The study aims to determine whether, after two months of supplementation:
- clinical symptoms improve
- quality of life increases
- intestinal inflammation decreases
- the gut microbiota shows a more balanced profile In parallel, the safety and tolerability of the supplement will be carefully evaluated.
Why is this study important?
If proven effective and safe, ButyMixx could become:
- a natural adjunct to pharmacological therapy
- a tool to support long-term intestinal health
- a strategy to reduce disease burden and improve daily well-being in patients with ulcerative colitis Contributing to a more comprehensive and preventive approach to disease management
Type d'étude
Inscription (Estimé)
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
- Nom: Sonia Facchin
- E-mail: sonia.facchin@unipd.it
Sauvegarde des contacts de l'étude
- Nom: Edoardo V Savarino
- Numéro de téléphone: 00390498127749
- E-mail: edoardo.savarinoi@unipd.it
Lieux d'étude
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Padova, Italie, 352121
- Recrutement
- Edoardo Savarino
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Contact:
- Edoardo Savarino
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Diagnosis of UC confirmed by clinical, endoscopic and histopathological evidence. Disease in remission phase confirmed by clinical, endoscopic and histopathological evidence.
- Age between 18 and 75 years old
- Ability of subject to participate fully in all aspects of this clinical trial.
Exclusion Criteria:
- Patients that have active UC, determined by clinical, endoscopic and histopathological evidence
- Known diagnosis of CD( Crohn disease), indeterminate colitis, ischemic colitis, radiation colitis, diverticular disease associated with colitis or microscopic colitis
- Positive stool culture for active C. difficile
- Pregnant women
- Patients under antibiotic and/or probiotic treatment within 10 days prior to Visit 1.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Autre: Butimixx
single arm
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Patients will be treated with the ButyMixx , a stick pack probiotic supplement composed sodium butyrate and the yeast Kluyveromyces marxianus, as primary compounds (300 mg and 33.5 mg rispectively).Patients will be asked to take 2 stick packs per day, before meals for 8 weeks.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Assessment of the clinical effectiveness of ButyMixx
Délai: 8 weeks
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The primary outcome is defined as the assessment of the clinical effectiveness of ButyMixx through a pre-post improvement (T0 vs T1) in at least one of the following three parameters: Partial Mayo Score (pMayo) - a clinical index measuring ulcerative colitis activity, including stool frequency, rectal bleeding, and physician's global assessment. IBDQ (Inflammatory Bowel Disease Questionnaire) - a validated questionnaire assessing disease-related quality of life. Fecal calprotectin (fCal) - an objective biomarker of intestinal inflammation. The primary outcome is therefore considered achieved if, after 8 weeks of supplementation, a clinically and statistically significant improvement is observed in at least one of these three indicators |
8 weeks
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Safety and tolerability
Délai: 8 weeks
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The secondary outcome is represented by the assessment of the safety and tolerability of the ButyMixx supplement. Systematic recording of adverse events (AEs) and serious adverse events (SAEs) All clinical events occurring during the study period are recorded according to standardized regulatory definitions and criteria. This allows assessment of whether ButyMixx intake is associated with undesirable effects and enables estimation of their frequency, type, and severity. Exploratory analysis of the intestinal microbiota Modulation of the microbiota profile is evaluated through 16S rRNA gene sequencing, and ITS(Internal Transcribed Spacer) sequencing for bacteria and fungi, with particular attention to the presence and dynamics of yeast species. This component is not intended as an efficacy endpoint, but rather as a tool to confirm that supplementation does not induce potentially unfavorable microbiological alterations, thereby strength |
8 weeks
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Edoardo V Savarino, Università degli Studi di Padova, DiSCOG
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 6440/AO/25
Plan pour les données individuelles des participants (IPD)
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Description du régime IPD
Informations sur les médicaments et les dispositifs, documents d'étude
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