Clinical Trials
11
Total Trials
9
Recruiting
1
With Results
Recent Trials
Genetic Characterization of Movement Disorders and Dementias
NCT02014246Recruiting12,000 enrolled
Human Movement Database
NCT00001252Recruiting7,500 enrolled
Botulinum Toxin for the Treatment of Involuntary Movement Disorders
NCT00001208Recruiting2,000 enrolled
Analysis of Cutaneous Phosphorylated Alpha-Synuclein to Identify Patients at Risk of Progressing From Essential Tremor to Parkinson's Disease
NCT07428447Recruiting300 enrolled
Deep Brain Stimulation Therapy in Movement Disorders
NCT02119611N/ARecruiting300 enrolled
Related Conditions
Mirror movements(child)
Oral dyskinesia(child)
Painful legs and moving toes(child)
Myoclonic disorder(child)
Grimace(child)
Medication-induced movement disorder(child)
Stiff-man syndrome(child)
Tic disorder(child)
Paradoxical facial movements(child)
Extrapyramidal disease(child)
Ballismus(child)
Apraxia due to cerebrovascular accident(child)
Benign shuddering attacks(child)
Organic sleep related movement disorder(child)
Essential tremor(child)
Deafness-dystonia syndrome(child)
Primary progressive freezing gait syndrome(child)
Primary orthostatic tremor(child)
Chronic hiccup(child)
Hereditary geniospasm(child)
Quick Facts
- SNOMED CT
- 60342002
- UMLS CUI
- C0026650
- Fully Specified Name
- Movement disorder (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- Clinical Trials
- 11
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.