Cure8

Why This Matters

This trial examines whether a blueberry-rich supplement can change inflammation, the microbiome, and intestinal barrier function in people with chronic colitis — topics many with IBD care about because diet and the microbiome may affect symptoms and disease activity.

Who Should Pay Attention

Adults with ulcerative colitis or Crohn’s colitis, patients interested in diet-based therapies, clinicians focused on nutritional/integrative care, and researchers studying microbiome–barrier interactions.

Study Snapshot

Story typeClinical Reference
Trial phaseNA
Enrollment60 participants
Study statusRecruiting
Source depthTrial registry record

What To Know

The study enrolls inpatients at a German integrative medicine clinic and uses a crossover design so each participant spends 3 months on supplemental blueberry powder and 3 months without it.

Researchers collect colonoscopy (with confocal laser endomicroscopy) and optional sigmoidoscopy biopsies, blood, urine, stool and bile samples, questionnaires, and symptom/stool diaries at baseline, 12 and 24 weeks to examine microbiome, barrier integrity, inflammation, and patient-reported outcomes.

The trial pairs clinical sampling with ex vivo and molecular analyses to explore mechanisms linking blueberry components (polyphenols, anthocyanins, fiber) to microbiome and barrier effects. The intervention is dietary (about 35 g blueberry powder daily) added to an existing integrative inpatient program; it is not a drug trial.

Keep In Mind

The record is a registered interventional crossover trial recruiting at a single center and focuses on mechanistic outcomes (biopsies, molecular analyses) alongside patient-reported measures. As an exploratory study, findings would be preliminary and hypothesis-generating.

Source Details

Review the original publication for the complete reporting, methods, and context.

Read Original Source
Clinical trial Evidence type derived from source or registry metadata.
PublicationClinicalTrials.gov
SponsorUniversität Duisburg-Essen
Trial IDNCT06698601
Study typeInterventional
Trial phaseNA
Enrollment60 participants
Indexed viaClinicalTrials.gov
Source typeTrial registry record
PublishedOct 1, 2026, 12:00 AM
Content availableTrial registry record

This Cure8 brief is based on source text from the linked article. Cure8 is informational only and is not a substitute for professional medical advice, diagnosis, or treatment.

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