Clinical Trials: Nutritional and Metabolic Diseases
- Abetalipoproteinemia 3 studies
- Achlorhydria 4 studies
- Acid-Base Imbalance 50 studies
- Acidosis 56 studies
- Acidosis, Lactic 22 studies
- Acidosis, Renal Tubular 2 studies
- Acidosis, Respiratory 1 study
- Adrenal Hyperplasia, Congenital 45 studies
- Adrenoleukodystrophy 14 studies
- Albinism 12 studies
- Albinism, Ocular 1 study
- Albinism, Oculocutaneous 7 studies
- Alkalosis 7 studies
- Alkaptonuria 3 studies
- Alpha-Mannosidosis 8 studies
- Amino Acid Metabolism, Inborn Errors 125 studies
- Amyloid Neuropathies 4 studies
- Amyloid Neuropathies, Familial 4 studies
- Amyloidosis 151 studies
- Amyloidosis, Familial 4 studies
- Amyotrophic Lateral Sclerosis 169 studies
- Anemia, Iron-Deficiency 169 studies
- Argininosuccinic Aciduria 2 studies
- Arthritis, Gouty 11 studies
- Ascorbic Acid Deficiency 2 studies
- Aspartylglucosaminuria 2 studies
- Ataxia Telangiectasia 10 studies
- Avitaminosis 271 studies
- Barth Syndrome 1 study
- Beriberi 5 studies
- Biotinidase Deficiency 1 study
- Blind Loop Syndrome 5 studies
- Bloom Syndrome 1 study
- Brain Diseases, Metabolic 398 studies
- Brain Diseases, Metabolic, Inborn 312 studies
- Calcinosis 106 studies
- Calciphylaxis 1 study
- Calcium Metabolism Disorders 227 studies
- Canavan Disease 4 studies
- Carbamoyl-Phosphate Synthase I Deficiency Disease 406 studies
- Celiac Disease 65 studies
- Cerebral Amyloid Angiopathy 2 studies
- Child Nutrition Disorders 8 studies
- Cholesterol Ester Storage Disease 10 studies
- Choline Deficiency 1 study
- Citrullinemia 5 studies
- Cockayne Syndrome 3 studies
- Colorectal Neoplasms, Hereditary Nonpolyposis 23 studies
- CREST Syndrome 4 studies
- Crigler-Najjar Syndrome 2 studies
- Cystinosis 15 studies
- Cystinuria 3 studies
- Deficiency Diseases 406 studies
- Dehydration 39 studies
- Dent Disease 2 studies
- Diabetes Mellitus 6269 studies
- Diabetes Mellitus, Experimental 1 study
- Diabetes Mellitus, Type 1 903 studies
- Diabetes Mellitus, Type 2 3277 studies
- Diabetes, Gestational 101 studies
- Diabetic Ketoacidosis 8 studies
- Dyslipidemias 1199 studies
- Fabry Disease 70 studies
- Fanconi Anemia 59 studies
- Fanconi Syndrome 60 studies
- Folic Acid Deficiency 3 studies
- Friedreich Ataxia 23 studies
- Frontotemporal Dementia 47 studies
- Frontotemporal Lobar Degeneration 40 studies
- Fructose Intolerance 2 studies
- Fucosidosis 6 studies
- Galactosemias 2 studies
- Gangliosidoses 11 studies
- Gangliosidoses, GM2 9 studies
- Gangliosidosis, GM1 4 studies
- Gaucher Disease 57 studies
- Gitelman Syndrome 2 studies
- Glucose Intolerance 278 studies
- Glucose Metabolism Disorders 6055 studies
- Glucosephosphate Dehydrogenase Deficiency 9 studies
- Glycogen Storage Disease 44 studies
- Glycogen Storage Disease Type II 42 studies
- Glycogen Storage Disease Type IV 1 study
- Glycogen Storage Disease Type VII 1 study
- Glycosuria, Renal 1 study
- Gout 80 studies
- Hemochromatosis 27 studies
- Hemosiderosis 20 studies
- Hepatic Encephalopathy 87 studies
- Hepatolenticular Degeneration 7 studies
- Hereditary Central Nervous System Demyelinating Diseases 34 studies
- Hermanski-Pudlak Syndrome 5 studies
- HIV Wasting Syndrome 14 studies
- HIV-Associated Lipodystrophy Syndrome 20 studies
- Homocystinuria 3 studies
- Hyperargininemia 1 study
- Hypercalcemia 33 studies
- Hypercholesterolemia 572 studies
- Hyperglycemia 498 studies
- Hyperhomocysteinemia 19 studies
- Hyperinsulinism 1092 studies
- Hyperkalemia 11 studies
- Hyperlipidemia, Familial Combined 24 studies
- Hyperlipidemias 898 studies
- Hyperlipoproteinemia Type I 6 studies
- Hyperlipoproteinemia Type II 58 studies
- Hyperlipoproteinemia Type III 3 studies
- Hyperlipoproteinemia Type IV 5 studies
- Hyperlipoproteinemia Type V 2 studies
- Hyperlipoproteinemias 77 studies
- Hypernatremia 12 studies
- Hyperoxaluria, Primary 8 studies
- Hyperphosphatemia 76 studies
- Hypertriglyceridemia 132 studies
- Hypoalphalipoproteinemias 5 studies
- Hypobetalipoproteinemias 6 studies
- Hypocalcemia 106 studies
- Hypoglycemia 217 studies
- Hypokalemia 11 studies
- Hypokalemic Periodic Paralysis 2 studies
- Hypolipoproteinemias 11 studies
- Hyponatremia 62 studies
- Hypophosphatasia 10 studies
- Hypophosphatemia 17 studies
- Hypophosphatemia, Familial 9 studies
- Hypophosphatemic Rickets, X-Linked Dominant 8 studies
- Ichthyosis, X-Linked 18 studies
- Inappropriate ADH Syndrome 12 studies
- Infant Nutrition Disorders 9 studies
- Insulin Resistance 1257 studies
- Iron Metabolism Disorders 260 studies
- Iron Overload 115 studies
- Ketosis 20 studies
- Kwashiorkor 8 studies
- Lactose Intolerance 11 studies
- Lesch-Nyhan Syndrome 3 studies
- Leukodystrophy, Globoid Cell 12 studies
- Leukodystrophy, Metachromatic 16 studies
- Li-Fraumeni Syndrome 22 studies
- Liddle Syndrome 1 study
- Lipid Metabolism Disorders 1378 studies
- Lipid Metabolism, Inborn Errors 296 studies
- Lipidoses 175 studies
- Lipodystrophy 98 studies
- Lipodystrophy, Congenital Generalized 2 studies
- Lipomatosis 7 studies
- Lipomatosis, Multiple Symmetrical 1 study
- Lysosomal Storage Diseases 285 studies
- Lysosomal Storage Diseases, Nervous System 201 studies
- Malabsorption Syndromes 128 studies
- Malnutrition 864 studies
- Mannosidase Deficiency Diseases 8 studies
- Maple Syrup Urine Disease 1 study
- MELAS Syndrome 8 studies
- Menkes Kinky Hair Syndrome 2 studies
- Metabolic Diseases 8986 studies
- Metabolic Syndrome X 646 studies
- Metabolism, Inborn Errors 841 studies
- Metal Metabolism, Inborn Errors 60 studies
- Mevalonate Kinase Deficiency 2 studies
- Mineralocorticoid Excess Syndrome, Apparent 2 studies
- Mitochondrial Diseases 80 studies
- Mitochondrial Encephalomyopathies 6 studies
- Mitochondrial Myopathies 9 studies
- Mucolipidoses 5 studies
- Mucopolysaccharidoses 60 studies
- Mucopolysaccharidosis I 26 studies
- Mucopolysaccharidosis II 15 studies
- Mucopolysaccharidosis III 7 studies
- Mucopolysaccharidosis IV 58 studies
- Mucopolysaccharidosis VI 14 studies
- Mucopolysaccharidosis VII 2 studies
- Nephrocalcinosis 5 studies
- Neuronal Ceroid-Lipofuscinoses 10 studies
- Niemann-Pick Disease, Type A 14 studies
- Niemann-Pick Disease, Type B 1 study
- Niemann-Pick Disease, Type C 14 studies
- Niemann-Pick Diseases 14 studies
- Nutrition Disorders 2893 studies
- Obesity 2773 studies
- Obesity Hypoventilation Syndrome 12 studies
- Obesity, Abdominal 60 studies
- Obesity, Morbid 181 studies
- Oculocerebrorenal Syndrome 3 studies
- Optic Atrophy, Autosomal Dominant 3 studies
- Optic Atrophy, Hereditary, Leber 7 studies
- Ornithine Carbamoyltransferase Deficiency Disease 7 studies
- Osteomalacia 15 studies
- Overnutrition 2306 studies
- Paralyses, Familial Periodic 3 studies
- Paralysis, Hyperkalemic Periodic 1 study
- Pelizaeus-Merzbacher Disease 3 studies
- Peroxisomal Disorders 17 studies
- Persistent Hyperinsulinemia Hypoglycemia of Infancy 7 studies
- Phenylketonuria, Maternal 1 study
- Phenylketonurias 41 studies
- Piebaldism 3 studies
- Porphyria Cutanea Tarda 4 studies
- Porphyria, Acute Intermittent 3 studies
- Porphyria, Erythropoietic 19 studies
- Porphyrias 19 studies
- Porphyrias, Hepatic 13 studies
- Potassium Deficiency 11 studies
- Prader-Willi Syndrome 22 studies
- Prediabetic State 164 studies
- Primary Progressive Nonfluent Aphasia 1 study
- Progeria 5 studies
- Propionic Acidemia 2 studies
- Protein Deficiency 15 studies
- Protein-Energy Malnutrition 14 studies
- Protoporphyria, Erythropoietic 6 studies
- Pseudohypoaldosteronism 4 studies
- Pseudohypoparathyroidism 6 studies
- Pseudopseudohypoparathyroidism 6 studies
- Refeeding Syndrome 1 study
- Refsum Disease 2 studies
- Refsum Disease, Infantile 2 studies
- Renal Osteodystrophy 14 studies
- Renal Tubular Transport, Inborn Errors 85 studies
- Rickets 53 studies
- Rothmund-Thomson Syndrome 1 study
- Sandhoff Disease 7 studies
- Scurvy 2 studies
- Severe Combined Immunodeficiency 39 studies
- Smith-Lemli-Opitz Syndrome 14 studies
- Sphingolipidoses 159 studies
- Sprue, Tropical 3 studies
- Starvation 8 studies
- Steatorrhea 14 studies
- Swayback 2 studies
- Tangier Disease 1 study
- Tay-Sachs Disease 10 studies
- Tetany 220 studies
- Thiamine Deficiency 5 studies
- Tyrosinemias 2 studies
- Urea Cycle Disorders, Inborn 42 studies
- Vitamin A Deficiency 17 studies
- Vitamin B 12 Deficiency 17 studies
- Vitamin B 6 Deficiency 1 study
- Vitamin D Deficiency 222 studies
- Wasting Syndrome 16 studies
- Water Intoxication 11 studies
- Water-Electrolyte Imbalance 155 studies
- Werner Syndrome 1 study
- Wernicke Encephalopathy 3 studies
- Wolfram Syndrome 1 study
- Wolman Disease 10 studies
- Xanthomatosis 3 studies
- Xanthomatosis, Cerebrotendinous 2 studies
- Xeroderma Pigmentosum 7 studies
- Zellweger Syndrome 2 studies
Clinical Trials content is provided directly by the U.S. National Institutes of Health via ClinicalTrials.gov and is not reviewed separately by ClinicalTrialsFeeds.org. Every page of specific clinical trials information contains a unique identifier which can be used to find further details directly from the National Institutes of Health.
The URL of this page is:
http://www.clinicaltrialsfeeds.org/clinical-trials/browse/cond_cat_BC18
