2 completed, 1 active not recruiting. 2 Not applicable.
| Phase | Trials | Status |
|---|---|---|
| Not applicable | 2 | Completed 2 |
Follow Hereditary Fructose Intolerance: new trials by email Literature Review of Hereditary Fructose Intolerance trials Research Report on Hereditary Fructose Intolerance
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 |
|---|---|---|---|---|---|---|
| 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 | |
| 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 |
Fructose Intolerance (3) · 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (1) · 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (1) · 3-methylcrotonyl CoA carboxylase 1 deficiency (1) · 3-methylcrotonyl CoA carboxylase 2 deficiency (1) · Acidemia, isovaleric (1) · Acrodermatitis enteropathica (1) · Adenine phosphoribosyltransferase deficiency (1) · Adrenal hyperplasia, congenital, type 5 (1) · Adrenocorticotropic hormone deficiency (1) · Amaurosis congenita of Leber, type 2 (1) · Anemia, Sickle Cell (1) · Angelman Syndrome (1) · Aortic Stenosis, Supravalvular (1) · Arginine-Glycine Amidinotransferase Deficiency (1)
Carbohydrate Metabolism, Inborn Errors (3) · Congenital, Hereditary, and Neonatal Diseases and Abnormalities (3) · Genetic Diseases, Inborn (3) · Metabolic Diseases (3) · Metabolism, Inborn Errors (3) · Nutritional and Metabolic Diseases (3) · Fructose Metabolism, Inborn Errors (2) · Abnormalities, Multiple (1) · Albinism (1) · Albinism, Oculocutaneous (1) · Amino Acid Metabolism, Inborn Errors (1) · Anemia (1) · Anemia, Hemolytic (1) · Anemia, Hemolytic, Congenital (1) · Aortic Valve Disease (1)
University of Lausanne (2) · RTI International (1)
Belgium (1) · United States (1)
Curt Scharfe, MD, PhD (1) · Tappy Luc, MD (1)
PMID 29955837, PMID 31315600, PMID 33551217, PMID 35142618
2016 (1)