Biocodex
Biocodex
Explore linked clinical trials.5 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Effects of Probiotic Consumption in Children With Autism Spectrum Disorder (ASD) | autism spectrum disorder, neurodevelopmental disorder, pervasive developmental disorder, psychiatric disorder | Active, not recruiting | Phase 2 | 2026-01-15 | NCT06568588 | |
| Probiotic and Ginger Supplement for Symptoms and Quality of Life in Functional Dyspepsia (SUBTILE) | Functional Dyspepsia | Recruiting | Not applicable | 2026-01-07 | NCT07212907 | |
| Saccharomyces Boulardii CNCM I-745 in Irritable Bowel Syndrome | Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Infant, Newborn, Diseases, Skin Abnormalities, Skin and Connective Tissue Diseases, colonic disorder, digestive system disorder, functional colonic disease, hereditary disease, hereditary skin disorder, ichthyosis, intestinal disorder, irritable bowel syndrome, keratosis, skin disorder, superficial epidermolytic ichthyosis | Recruiting | Phase 3 | 2025-11-18 | NCT07168434 | |
| Effect of Saccharomyces Boulardii CNCM I-745 on Gut Microbiota in Patients Undergoing Antibiotic Therapy (in the Context of Erythema Migrans (Early Skin Form of Lyme Borreliosis)) | Bacterial Infections and Mycoses, Borrelia infectious disease, Erythema, Erythema Chronicum Migrans, Glossitis, Benign Migratory, Infections, Lyme disease, Skin and Connective Tissue Diseases, Stomatognathic Diseases, bacterial infectious disease, glossitis, gram-negative bacterial infections, mouth disorder, skin disease caused by bacterial infection, skin disorder, skin disorder caused by infection, spirochaetales infections, tick-borne infectious disease, tongue disorder, vector-borne disease | Recruiting | Phase 4 | 2025-08-27 | NCT06451913 | |
| Evaluation of the Efficacy and Safety of Stiripentol in Patients 6 Years and Older With Primary Hyperoxaluria Type 1, 2 or 3 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hyperoxaluria, Male Urogenital Diseases, Nutritional and Metabolic Diseases, Urogenital Diseases, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, kidney disorder, metabolic disease, primary hyperoxaluria, primary hyperoxaluria type 1, primary hyperoxaluria type 2, primary hyperoxaluria type 3, urinary system disorder | Not yet recruiting | Phase 3 | 2024-06-18 | NCT06465472 |