- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07646223
Vancomycin Efficacy in Response to Dysbiosis in Atypical Colitis (VERDA)
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:
- Does oral vancomycin improve disease activity and lead to remission (based on symptoms, biomarkers, and endoscopy findings)?
- How does oral vancomycin change gut metabolism?
- 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:
- Take oral vancomycin (if assigned) together with conventional treatment for at least 3 months and up to 12 months depending on response
- Visit the clinic approximately every 3 months for checkups, tests, and monitoring
- Provide blood, stool, and saliva samples to study disease activity and microbiota activity
- Undergo clinical assessments such as symptom scoring, imaging, and possibly endoscopy
- Complete questionnaires about quality of life
- Be monitored for side effects and treatment response throughout the study period
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
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:
- 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?
- How does oral vancomycin change the gut microbiota and hut metabolism, and are these changes linked to treatment response?
- Does oral vancomycin improve liver-related outcomes in children with PSC-UC (e.g., liver enzymes and liver stiffness)?
- Does treatment improve the quality of life of children and their families?
- 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.
Type d'étude
Inscription (Estimé)
Phase
- Phase 2
Contacts et emplacements
Coordonnées de l'étude
- Nom: Laura Räisänen, PhD
- Numéro de téléphone: +358444735309
- E-mail: laura.raisanen@pirha.fi
Lieux d'étude
-
-
-
Tampere, Finlande
- Tampere University Hospital
-
Contact:
- Saara Ojala
- E-mail: saara.ojala@pirha.fi
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
Accepte les volontaires sains
La description
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 d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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.
|
|
Comparateur actif: 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.
|
|
Aucune intervention: Children with atypical UC without confirmed PSC receiving conventional treatment only
PSC is not seen in MRCP, will not receive oral vancomycin
|
|
|
Aucune intervention: Children with typical UC without confirmed PSC receiving conventional treatment only
Typical UC in colonoscopy, will not receive oral vancomycin
|
|
|
Aucune intervention: Children without IBD
Control group for healthy gut microbiota and non-inflammatory gut metabolism
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Colitis remission
Délai: 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
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change in ALT levels
Délai: 6 to 12 months
|
6 to 12 months
|
|
|
Change in the GGT levels
Délai: 6-12 months
|
6-12 months
|
|
|
Change in the liver stiffness
Délai: 6-12 months
|
Measured using shear wave elastography
|
6-12 months
|
|
Changes in the MRCP findings pre-post OVT
Délai: 12 months
|
12 months
|
Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Changes in gut microbiota and gut metabolism
Délai: 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
|
Collaborateurs et enquêteurs
Parrainer
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
Mots clés
Termes MeSH pertinents supplémentaires
- Maladies intestinales
- Maladies du système digestif
- Maladies gastro-intestinales
- Maladies des voies biliaires
- Maladies du côlon
- Gastro-entérite
- Maladies intestinales inflammatoires
- Maladies des voies biliaires
- Cholangite
- Colite
- Colite ulcéreuse
- Cholangite, sclérosante
- Peptides
- Acides aminés, peptides et protéines
- Glucides
- Glycoconjuguis
- Glycopeptides
- Vancomycine
Autres numéros d'identification d'étude
- R26052M
- 2025 (Subvention/contrat des NIH des États-Unis: Faculty of Social Sciences Scientific Grant at the University of Gdańsk)
- 2025-524543-12-00 (Ctis)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
produit fabriqué et exporté des États-Unis.
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .