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Explore conditions, clinical trials, and the organisations running them.

Movement disorder

Neurological conditions resulting in abnormal voluntary or involuntary movement, which may impact the speed, fluency, quality and ease of movement.

108 trials tagged with this condition →

Extrapyramidal and movement disease 0 trials · 149 incl. sub-types Sub-types →
Cerebellar ataxia 40 trials · 144 incl. sub-types Sub-types →
Multiple system atrophy 110 trials · 119 incl. sub-types Sub-types →
Essential tremor 102 trials · 104 incl. sub-types Sub-types →
Progressive supranuclear palsy 73 trials · 77 incl. sub-types Sub-types →
Huntington disease 76 trials Sub-types →
Progressive non-fluent aphasia 23 trials · 44 incl. sub-types Sub-types →
Behavioral variant of frontotemporal dementia 21 trials · 42 incl. sub-types Sub-types →
Tourette syndrome 41 trials
Corticobasal syndrome 19 trials
Frontotemporal dementia with motor neuron disease 13 trials · 19 incl. sub-types Sub-types →
Chronic tic disorder 15 trials
Choreatic disease 11 trials Sub-types →
Neurodegeneration with brain iron accumulation 1 trial · 8 incl. sub-types Sub-types →
Arthrogryposis 4 trials · 6 incl. sub-types Sub-types →
Inherited Creutzfeldt-Jakob disease 5 trials
Primary orthostatic tremor 5 trials
Clonic hemifacial spasm 4 trials
Familial congenital mirror movements 3 trials Sub-types →
Transient tic disorder 3 trials
Dyskinesia with orofacial involvement, autosomal dominant 2 trials
Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome 2 trials
Opsoclonus-myoclonus syndrome 2 trials
Lafora disease 1 trial Sub-types →
Unverricht-Lundborg syndrome 1 trial
Benign shuddering attacks 1 trial
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder 1 trial
Myoclonus, familial 1 trial Sub-types →
Neuronal intranuclear inclusion disease 1 trial
Psychogenic movement disorders 1 trial
PRRT2-associated paroxysmal movement disorder 0 trials · 1 incl. sub-types Sub-types →
Intellectual disability-hyperkinetic movement-truncal ataxia syndrome 0 trials · 1 incl. sub-types Sub-types →
Huntington disease-like 3 0 trials
Huntington disease-like syndrome due to C9ORF72 expansions 0 trials
SLC6A3-related dopamine transporter deficiency syndrome 0 trials Sub-types →
Sandifer syndrome 0 trials
Benign paroxysmal tonic upgaze of childhood with ataxia 0 trials
Brain-lung-thyroid syndrome 0 trials
Childhood-onset benign chorea with striatal involvement 0 trials
Complex movement disorder with or without neurodevelopmental features 0 trials Sub-types →
Epilepsy with myoclonic absences 0 trials
Hereditary geniospasm 0 trials
Hyperekplexia 0 trials Sub-types →
Isolated facial myokymia 0 trials
Kuru 0 trials
Lingual-facial-buccal dyskinesia 0 trials
Neuroacanthocytosis 0 trials Sub-types →
Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome 0 trials
Progressive myoclonic epilepsy type 7 0 trials
Proximal myopathy with extrapyramidal signs 0 trials
Sensorineural hearing loss-early graying-essential tremor syndrome 0 trials
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome 0 trials
Tremor-nystagmus-duodenal ulcer syndrome 0 trials
Variably protease-sensitive prionopathy 0 trials