2 unknown, 1 completed. .
Follow Malonic aciduria: new trials by email Literature Review of Malonic aciduria trials Research Report on Malonic aciduria
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 |
|---|---|---|---|---|---|---|
| Selective Screening of Children for Hereditary Metabolic Diseases by Tandem Mass Spectrometry in Kazakhstan Obtaining Dry Blood Spots From Healthy Newborns (Aged 1-7 Days), Obtaining Dry Blood Spots From Healthy Children Aged 8 Days - 7 Years, Obtaining Dry Blood Spots From Healthy Children Aged 8-18 Years - Propionic/Methylmalonic Acidemias, Maple Syrup Urine Disease | Unknown | West Kazakhstan Medical University | 2250 | 2022-10-03 | 2023-06-18 | |
| 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 | |
| Combined Malonic and Methylmalonic Aciduria (CMAMMA): Gene Identification and Outcome Study Malonic Aciduria, Methylmalonic Acidemia | Unknown | McGill University Health Centre/Research Institute of the McGill University Health Centre | 6 | 2011-02-01 | 2011-02-08 |
3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (2) · Acidemia, isovaleric (2) · Argininosuccinic Aciduria (2) · Beta ketothiolase deficiency (2) · Biotinidase Deficiency (2) · Carbamoyl-Phosphate Synthase I Deficiency Disease (2) · Carnitine palmitoyl transferase 1A deficiency (2) · Carnitine palmitoyl transferase 2 deficiency (2) · Carnitine-Acylcarnitine Translocase Deficiency (2) · Citrullinemia (2) · Glutaric Acidemia I (2) · Homocystinuria (2) · Hyperargininemia (2) · Hyperglycinemia, Nonketotic (2)
Amino Acid Metabolism, Inborn Errors (2) · Brain Diseases (2) · Brain Diseases, Metabolic (2) · Brain Diseases, Metabolic, Inborn (2) · Carbohydrate Metabolism, Inborn Errors (2) · Central Nervous System Diseases (2) · Congenital, Hereditary, and Neonatal Diseases and Abnormalities (2) · Connective Tissue Diseases (2) · Genetic Diseases, Inborn (2) · Genetic Diseases, X-Linked (2) · Hyperhomocysteinemia (2) · Metabolic Diseases (2) · Mitochondrial Diseases (2) · Multiple Carboxylase Deficiency (2) · Nervous System Diseases (2)
Aging (1)
Centre Hospitalier Universitaire de Liege (1) · McGill University Health Centre/Research Institute of the McGill University Health Centre (1) · West Kazakhstan Medical University (1)
Belgium (1) · Canada (1) · Kazakhstan (1)
Gulmira M. Zharmakhanova, MD, PhD (1) · Laurent Servais (1) · Lyazzat M. Syrlybayeva, MD (1) · Victoria I. Kononets, MD, MS (1)