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Explore conditions, clinical trials, and the organisations running them.
7285 conditions with clinical trials.
- Acquired hemophilia A 17 trials
- Acute bronchiolitis 17 trials
- Acute kidney tubular necrosis 17 trials
- Amyotrophic lateral sclerosis type 1 17 trials
- Angelman syndrome 17 trials
- Antisocial personality disorder 17 trials
- Apnea of prematurity 17 trials
- Arthrogryposis 17 trials
- Asherman syndrome 17 trials
- Autism spectrum disorder 1 17 trials
- Autosomal recessive spinocerebellar ataxia 7 17 trials
- Candidiasis, invasive 17 trials
- Carotid artery occlusion 17 trials
- Carotid artery thrombosis 17 trials
- Charlevoix-Saguenay spastic ataxia 17 trials
- Chronic conjunctivitis 17 trials
- Chronic rapidly progressive glomerulonephritis 17 trials
- COACH syndrome 17 trials
- Congenital fibrinogen deficiency 17 trials
- Congenital herpes virus infection 17 trials
- Congenital primary aphakia 17 trials
- Congenital vitamin K-dependent coagulation factors deficiency 17 trials
- Corneal ectasia 17 trials
- Deafness, aminoglycoside-induced 17 trials
- Deficiency of adenosine deaminase 2 17 trials
- Developmental and epileptic encephalopathy, 11 17 trials
- Developmental and epileptic encephalopathy, 13 17 trials
- Developmental and epileptic encephalopathy, 14 17 trials
- Distal hereditary motor neuropathy 17 trials
- Dumping syndrome 17 trials
- Dystocia 17 trials
- Esophageal atresia 17 trials
- Exotropia 17 trials
- Familial dysfibrinogenemia 17 trials
- Friedreich ataxia 1 17 trials
- Gaucher disease type I 17 trials
- Hemarthrosis 17 trials
- Histoplasmosis retinitis 17 trials
- Homocystinuria without methylmalonic aciduria 17 trials
- Hypophosphatemic rickets 17 trials
- Idiopathic achalasia 17 trials
- Infantile epileptic-dyskinetic encephalopathy 17 trials
- Inherited Creutzfeldt-Jakob disease 17 trials
- Iris hypoplasia with glaucoma 17 trials
- Joubert syndrome with oculorenal defect 17 trials
- Limbal stem cell deficiency 17 trials
- Macrocytic anemia 17 trials
- Methylcobalamin deficiency type cblE 17 trials
- Methylcobalamin deficiency type cblG 17 trials
- Methylmalonic aciduria and homocystinuria type cblD 17 trials