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Vancomycin Efficacy in Response to Dysbiosis in Atypical Colitis (VERDA)

7 de septiembre de 2026 actualizado por: Tampere University Hospital

The Efficacy of Oral Vancomycin Therapy in Managing Different Phenotypes of Paediatric Inflammatory Bowel Diseases by Correlating Treatment Response to Commensal Microbiota Composition and Function

The goal of this clinical trial is to learn how oral vancomycin therapy may contribute in treating paediatric inflammatory bowel disease, particularly atypical ulcerative colitis and PSC-associated colitis. It will also give more information on how this treatment affects gut microbiota and metabolism.

The main questions it aims to answer are:

  1. Does oral vancomycin improve disease activity and lead to remission (based on symptoms, biomarkers, and endoscopy findings)?
  2. How does oral vancomycin change gut metabolism?
  3. Does different types of colitis respond differently to oral vancomycin?

Researchers will compare children receiving oral vancomycin plus standard therapy to those receiving standard therapy alone. The gut metabolisim before and after oral vancmycin will also be compared, as well as to healthy controls and children with typical ulcerative colitis.

Participants will:

  1. Take oral vancomycin (if assigned) together with conventional treatment for at least 3 months and up to 12 months depending on response
  2. Visit the clinic approximately every 3 months for checkups, tests, and monitoring
  3. Provide blood, stool, and saliva samples to study disease activity and microbiota activity
  4. Undergo clinical assessments such as symptom scoring, imaging, and possibly endoscopy
  5. Complete questionnaires about quality of life
  6. Be monitored for side effects and treatment response throughout the study period

Descripción general del estudio

Descripción detallada

The goal of this clinical trial is to learn whether oral vancomycin therapy could be used to treat paediatric inflammatory bowel diseases (IBD), particularly atypical ulcerative colitis and ulcerative colitis associated with primary sclerosing cholangitis (PSC-UC). This trial will also investigate how oral vancomycin may affect gut microbiota (the community of bacteria in the gut) and change gut metabolism, influence disease progression, and exhibit overall safety during long-term use.

The main questions it aims to answer are:

  1. Does oral vancomycin improve disease activity and lead to remission based on clinical symptoms (PUCAI score), biomarkers (such as faecal calprotectin), imaging, and endoscopy findings?
  2. How does oral vancomycin change the gut microbiota and hut metabolism, and are these changes linked to treatment response?
  3. Does oral vancomycin improve liver-related outcomes in children with PSC-UC (e.g., liver enzymes and liver stiffness)?
  4. Does treatment improve the quality of life of children and their families?
  5. What medical problems, side effects, or risks do participants have when taking oral vancomycin, including the development of antibiotic-resistant bacteria?

Researchers will compare groups of children receiving oral vancomycin together with conventional medical treatment (CMT) to those receiving conventional treatment alone in certain patient groups. They will also compare stool and gut metabolims findings with children who have typical ulcerative colitis, and with healthy controls.

The participants will:

  • Be children aged 6-15 years who are planned for colonoscopy due to suspected inflammatory bowel disease
  • Be assigned to different groups based on their colonoscopy results (e.g., PSC-UC, atypical UC without PSC, typical UC, or healthy controls); children with atypical UC will be randomly assigned to receive oral vancomycin plus conventional treatment or conventional treatment alone
  • Take oral vancomycin capsules (if assigned) in addition to standard therapy, typically three times per day, for at least 3 months and up to 12 months depending on treatment response
  • Continue standard treatments for IBD (such as mesalazine, thiopurines, or biologics) as part of routine care

Participants will attend clinic visits and follow-ups at baseline (before treatment) and then approximately every 3 months (at 3, 6, 9, and 12 months) while receiving oral vancomycin. After ceasing oral vancomycin, they will be followed-up for another 12 months - up to 2 years after the start of the study

During the study, participants will undergo a range of clinical assessments and tests, including:

  • Symptom assessment using the Paediatric Ulcerative Colitis Activity Index (PUCAI)
  • Blood tests to monitor inflammation, liver function, and general health
  • Stool samples to measure faecal calprotectin and analyse gut microbiota
  • Saliva samples to study microbiota composition
  • Imaging tests such as intestinal ultrasound (to measure bowel wall thickness) and liver elastography (to assess liver stiffness)
  • Magnetic resonance imaging (MRCP) in selected patients to assess bile duct disease
  • Endoscopy and biopsies (at baseline and, if needed, during follow-up) to evaluate intestinal inflammation and healing
  • Quality-of-life questionnaires completed by the child and/or their parents

Participants taking oral vancomycin will also be closely monitored for:

  • side effects, including gastrointestinal symptoms such as nausea or diarrhoea
  • Blood and stool testing will help identify potential complications, including development of vancomycin-resistant bacteria
  • Treatment may be stopped early if the participant does not respond or if significant side effects occur

Researchers will analyse changes over time in clinical outcomes, microbiota composition, gut metabolism, and laboratory findings to determine whether oral vancomycin is effective and safe. They will also investigate whether changes in the microbiome can predict which patients respond to treatment.

Overall, this study aims to improve understanding of paediatric IBD, especially atypical forms linked to PSC, and to evaluate whether modifying gut bacteria with oral vancomycin can lead to better disease control, improved quality of life, and more personalised treatment strategies for children.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

140

Fase

  • Fase 2

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

Ubicaciones de estudio

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

  • Niño

Acepta Voluntarios Saludables

No

Descripción

Inclusion criteria.

  • children aged 6-15 years
  • able to swallow capsules
  • are scheduled for diagnostic endoscopy at Tampere University
  • has not received oral vancomycin before
  • do not have active infection (such as clostridium or other bacteria)
  • has not received new interventions (medications or new conventional therapies) for treating IBD was given within the past 4 weeks before starting OVT.

Exclusion Criteria:

  • The presence of PSC without UC, Crohn's disease type of inflammatory bowel diseases.
  • Under the age of 6 years old.
  • Is unable to swallow capsules.
  • Had a previous allergic reaction to vancomycin (such as vancomycin allergy) and/or other related antibiotics similar to vancomycin.
  • Presence of malignant disease or potential need for liver transplantation within the following 12 months.
  • Pregnancy
  • Known renal insufficiency or chronic renal disease

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: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Children with ulcerative colitis and confirmed PSC receiving OVT and conventional treatment
PSC is confirmed with MRCP and/or biopsy, will receive oral vancomycin (OVT) for 3-6-(12) months depending on the clinical response
Oral vancomycin will be given 50 mg/ kg in three divided doses up to 500 mg x 3/ day for at least 3 months. In responding children, the treatment will be continued for 6(-12) months depending on the timing if possible follow-up colonoscopy.
Comparador activo: Children with atypical UC without confirmed PSC receiving OVt and conventional treatment
PSC is not seen in MRCP, will receive oral vancomycin for 3-6-(12) months depending on the clinical response.
Oral vancomycin will be given 50 mg/ kg in three divided doses up to 500 mg x 3/ day for at least 3 months. In responding children, the treatment will be continued for 6(-12) months depending on the timing if possible follow-up colonoscopy.
Sin intervención: Children with atypical UC without confirmed PSC receiving conventional treatment only
PSC is not seen in MRCP, will not receive oral vancomycin
Sin intervención: Children with typical UC without confirmed PSC receiving conventional treatment only
Typical UC in colonoscopy, will not receive oral vancomycin
Sin intervención: Children without IBD
Control group for healthy gut microbiota and non-inflammatory gut metabolism

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Colitis remission
Periodo de tiempo: 3 to 6 months
Remission is defined as PUCAI < 10, fecal calprotectin < 100 ug/g, and normal bowel wall thickness in all segments of the colon at intestinal ultrasound
3 to 6 months

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in ALT levels
Periodo de tiempo: 6 to 12 months
6 to 12 months
Change in the GGT levels
Periodo de tiempo: 6-12 months
6-12 months
Change in the liver stiffness
Periodo de tiempo: 6-12 months
Measured using shear wave elastography
6-12 months
Changes in the MRCP findings pre-post OVT
Periodo de tiempo: 12 months
12 months

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Changes in gut microbiota and gut metabolism
Periodo de tiempo: 6 to 12 months
Stool samples will be analyzed for gut microbiota diversity and biopsy samples for gut metabolism (using Olink proteomics)
6 to 12 months

Colaboradores e Investigadores

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

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 octubre de 2026

Finalización primaria (Estimado)

31 de diciembre de 2032

Finalización del estudio (Estimado)

31 de diciembre de 2035

Fechas de registro del estudio

Enviado por primera vez

4 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

9 de junio de 2026

Publicado por primera vez (Actual)

12 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

10 de septiembre de 2026

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

7 de septiembre de 2026

Última verificación

1 de junio 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

Ethical restriction

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

producto fabricado y exportado desde los 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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