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Explore conditions, clinical trials, and the organisations running them.
7285 conditions with clinical trials.
- Digitalis poisoning 4 trials
- Disorder of carnitine cycle and carnitine transport 4 trials
- Disorder of fucoglycosan synthesis 4 trials
- Disorder of galactose and fructose metabolism 4 trials
- Disorder of magnesium transport 4 trials
- Disorder of peptide and amine metabolism 4 trials
- Distal arthrogryposis 4 trials
- Drug-induced hearing loss 4 trials
- Drug-induced hepatitis 4 trials
- Drug-induced myopathy 4 trials
- Drug-induced osteoporosis 4 trials
- Echinococcus granulosus infectious disease 4 trials
- Endometrial hyperplasia without atypia 4 trials
- Endometrial polyp 4 trials
- Enlarged vestibular aqueduct syndrome 4 trials
- Enterococcus infectious disease 4 trials
- Epidermolytic ichthyosis 4 trials
- Excessive tearing 4 trials
- Exfoliation syndrome, susceptibility to 4 trials
- Expressive language disorder 4 trials
- Familial hyperaldosteronism 4 trials
- Familial primary localized cutaneous amyloidosis 4 trials
- Familial thyroid dyshormonogenesis 4 trials
- Fanconi renotubular syndrome 4 trials
- Filamin-related bone disorder 4 trials
- Food protein-induced enterocolitis syndrome 4 trials
- Fulminant viral hepatitis 4 trials
- Fusariosis 4 trials
- Gastric dilatation 4 trials
- Gaucher disease type II 4 trials
- Glaucoma 3A 4 trials
- Global developmental delay with or without impaired intellectual development 4 trials
- Glucocorticoid-induced osteoporosis 4 trials
- Glucocorticoid resistance 4 trials
- Glutaric aciduria 4 trials
- Glutaryl-CoA dehydrogenase deficiency 4 trials
- Growth delay due to insulin-like growth factor I resistance 4 trials
- Hallucinogen-persisting perception disorder 4 trials
- Hemorrhagic fever-renal syndrome 4 trials
- Hereditary vs non-hereditary etiology 4 trials
- Hernia, double inguinal 4 trials
- Histoplasmosis 4 trials
- HIV-associated nephropathy 4 trials
- HMBS-related hepatic porphyria 4 trials
- Hypercalcemia disease 4 trials
- Hypercholesterolemia, autosomal dominant, 3 4 trials
- Hyperreflexia 4 trials
- Hypocalcified amelogenesis imperfecta 4 trials
- Hypocomplementemic urticarial vasculitis 4 trials
- Hypophosphatemic rickets, autosomal recessive, 1 4 trials