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Sodium Butyrate and Kluyveromyces Marxianus Supplementation in Inflammatory Bowel Disease (Butymixx)

12 de mayo de 2026 actualizado por: Savarino Edoardo Vincenzo, University of Padova

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

Descripción general del estudio

Estado

Reclutamiento

Intervención / Tratamiento

Descripción detallada

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:

  1. 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.
  2. 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

Tipo de estudio

Intervencionista

Inscripción (Estimado)

40

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Copia de seguridad de contactos de estudio

Ubicaciones de estudio

      • Padova, Italia, 352121
        • Reclutamiento
        • Edoardo Savarino
        • Contacto:
          • Edoardo Savarino

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

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 de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Otro: Butimixx
single arm
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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Assessment of the clinical effectiveness of ButyMixx
Periodo de tiempo: 8 weeks

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

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Safety and tolerability
Periodo de tiempo: 8 weeks

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

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Investigador principal: Edoardo V Savarino, Università degli Studi di Padova, DiSCOG

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de mayo de 2026

Finalización primaria (Estimado)

31 de diciembre de 2026

Finalización del estudio (Estimado)

30 de marzo de 2027

Fechas de registro del estudio

Enviado por primera vez

13 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

12 de mayo de 2026

Publicado por primera vez (Actual)

15 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

15 de mayo de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

12 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

Individual participant data (IPD) will not be shared.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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