7 completed, 4 unknown, 1 active not recruiting, 1 not yet recruiting. 6 Not applicable, 1 Phase 2, 1 Phase 3.
| Phase | Trials | Status |
|---|---|---|
| Not applicable | 6 | Completed 3, Unknown 2, Not yet recruiting 1 |
| Phase 2 | 1 | Completed 1 |
| Phase 3 | 1 | Completed 1 |
Follow Fructose Metabolism, Inborn Errors: new trials by email Literature Review of Fructose Metabolism, Inborn Errors trials Research Report on Fructose Metabolism, Inborn Errors
Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.
| Trial | Phase | Status | Sponsor | Enrollment | Start | Updated |
|---|---|---|---|---|---|---|
| New Microbiota-endocrine Axis in Fructose Malabsorption-caused Visceral Hypersensitivity in Irritable Bowel Syndrome. urine intestinal permeability test or lactulose/mannitol test, Blood test, food diary - Irritable Bowel Syndrome (IBS) | Not applicable | Not yet recruiting | University Hospital, Rouen | 60 | 2026-02-01 | 2026-01-13 |
| Observational Study on the Safety and Efficacy of the Medical Product Fructosin. Fructosin - Fructose Intolerance | Unknown | Sciotec Diagnostic Technologies GmbH | 60 | 2023-10-01 | 2023-09-21 | |
| Baby Detect : Genomic Newborn Screening Congenital Adrenal Hyperplasia, Familial Hyperinsulinemic Hypoglycemia 1 | Completed | Centre Hospitalier Universitaire de Liege | 6824 | 2022-09-01 | 2025-08-12 | |
| Fructose and Lactose Intolerance and Malabsorption in Functional Gastrointestinal Disorders no intervention: observational study - Functional Gastrointestinal Disorders, Lactose Intolerance | Unknown | Brain-Gut Research Group | 3000 | 2019-03-01 | 2021-03-30 | |
| Early Check: Expanded Screening in Newborns Confirmatory Testing - Spinal Muscular Atrophy, Fragile X Syndrome | Active not recruiting | RTI International | 30000 | 2018-10-15 | 2026-07-01 | |
| Biomarker for Glycogen Storage Diseases (BioGlycogen) Fructose Metabolism, Inborn Errors, Glycogen Storage Disease | Withdrawn | CENTOGENE GmbH Rostock | 2018-08-20 | 2023-02-13 | ||
| Fructose Supplementation in Carriers for Hereditary Fructose Intolerance Experimental diet Fru rich diet, Experimental low Fru diet - Hereditary Fructose Intolerance | Not applicable | Completed | University of Lausanne | 12 | 2018-05-01 | 2019-04-22 |
| Metabolic Consequences of Heterozygous Hereditary Fructose Intolerance Test meal - Hereditary Fructose Intolerance, Fructose Metabolism, Inborn Errors | Not applicable | Completed | University of Lausanne | 18 | 2015-01-01 | 2019-07-17 |
| Investigation of Supplemental L-alanine in the Management of Dietary Fructose Intolerance Placedo, Alanine - Fructose Intolerance | Not applicable | Unknown | Augusta University | 65 | 2014-01-07 | 2020-04-15 |
| Is the Expression of the GLUT5 Specific Fructose Transport Protein Abnormal in Patients With Fructose Intolerance? Irritable Bowel Syndrome, Fructose Intolerance | Completed | Brain-Gut Research Group | 26 | 2011-12-01 | 2018-12-17 | |
| Clinical Utility of Breath Tests in GI Small Intestinal Bacterial Overgrowth, Lactose Intolerance | Completed | Augusta University | 1080 | 2011-08-31 | 2020-02-17 | |
| Efficacy of Fructose Metabolizing Enzymatic Product in Fructose Malabsorption Fructosin - Fructose Malabsorption | Not applicable | Completed | Sciotec Diagnostic Technologies GmbH | 65 | 2009-06-01 | 2010-12-20 |
| Investigation of Alanine in Fructose Intolerance: A Dose Ranging Study Placebo, Alanine - Fructose Intolerance | Not applicable | Unknown | Augusta University | 100 | 2007-09-01 | 2022-07-21 |
| Fructose Malabsorption in Northern Norway diet restriction - Irritable Bowel Syndrome, Fructose Malabsorption | Phase 2 / Phase 3 | Completed | University Hospital of North Norway | 182 | 2007-09-01 | 2016-05-24 |
Fructose Intolerance (13) · Glycogen Storage Disease Type II (3) · Irritable Bowel Syndrome (3) · 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (2) · Acidemia, isovaleric (2) · Anemia, Sickle Cell (2) · Argininosuccinic Aciduria (2) · Ataxia with vitamin E deficiency (2) · Basal ganglia disease, biotin-responsive (2) · Beta ketothiolase deficiency (2) · Biotinidase Deficiency (2) · Brown-Vialetto-Van Laere syndrome (2) · Carbamoyl-Phosphate Synthase I Deficiency Disease (2) · Carnitine palmitoyl transferase 1A deficiency (2) · Carnitine palmitoyl transferase 2 deficiency (2)
Carbohydrate Metabolism, Inborn Errors (14) · Congenital, Hereditary, and Neonatal Diseases and Abnormalities (14) · Genetic Diseases, Inborn (14) · Metabolism, Inborn Errors (14) · Nutritional and Metabolic Diseases (14) · Metabolic Diseases (13) · Digestive System Diseases (7) · Intestinal Diseases (5) · Gastrointestinal Diseases (4) · Bone Diseases (3) · Bone Diseases, Metabolic (3) · Brain Diseases (3) · Brain Diseases, Metabolic (3) · Brain Diseases, Metabolic, Inborn (3)
Alanine (2) · Diet Records (1) · Hematologic Tests (1) · Lactulose (1)
Augusta University (3) · Brain-Gut Research Group (2) · Sciotec Diagnostic Technologies GmbH (2) · University of Lausanne (2) · CENTOGENE GmbH Rostock (1) · Centre Hospitalier Universitaire de Liege (1) · RTI International (1) · University Hospital of North Norway (1) · University Hospital, Rouen (1)
United States (4) · Austria (2) · Belgium (2) · Switzerland (2) · France (1) · Germany (1) · India (1) · Norway (1) · Sri Lanka (1)
C Wilder-Smith, MD (1) · Christian Pongracz, MS (1) · Clive Wilder-Smith, MD (1) · Curt Scharfe, MD, PhD (1) · Jon Florholmen, MD PhD (1) · Laurent Servais (1) · Peter Bauer, Prof. (1) · Peter Komericki, MD (1) · Satish Rao, Md, PhD (1) · Satish SC Rao, MD, PhD (1) · Tappy Luc, MD (1)
PMID 25987795, PMID 29881615, PMID 29955837, PMID 30009815, PMID 31315600, PMID 32955198, PMID 33551217, PMID 35142618
2016 (1)