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Combined dystonia
MONDO:0020065A dystonia that is combined with another movement disorder (e.g., myoclonus, parkinsonism).
Also known as: dystonia-plus syndrome
26 clinical trials for this condition and its sub-types, 1 tagged with Combined dystonia itself.
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Sub-types of Combined dystonia
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Myoclonus-dystonia syndrome 3 trials
3 sub-types
- Myoclonic dystonia 11 0 trials
- Myoclonic dystonia 15 0 trials
- Myoclonic dystonia 26 0 trials
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Paroxysmal dystonia 0 trials · 3 incl. sub-types
3 sub-types
- Paroxysmal dyskinesia 1 trial · 3 incl. sub-types Sub-types →
- Benign paroxysmal torticollis of infancy 0 trials
- Dystonia 9 0 trials
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Dystonia 12 2 trials
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X-linked dystonia-parkinsonism 0 trials
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Ataxia - telangiectasia variant 0 trials
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Combined cervical dystonia 0 trials
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Dystonia 16 0 trials
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Dystonia-aphonia syndrome 0 trials
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Parkinsonism-dystonia, infantile 0 trials
3 sub-types
Most studied deeper sub-types
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New hope for kids with rare epilepsy: drug trial targets seizure control
Disease control OngoingThis study tests an investigational drug called relutrigine in 160 children with a severe form of epilepsy called developmental and epileptic encephalopathy (DEE). The goal is to see if the drug can safely reduce monthly seizure frequency compared to a placebo. After the initial …
Phase 3 • Sponsor: Praxis Precision Medicines • Aim: Disease control
Last updated Aug 06, 2026 00:00 UTC
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New program aims to ease burden on families of kids with rare diseases
Symptom relief By invitation onlyThis study tests a program called FACE-Rare, designed to support family caregivers of children with rare, life-limiting diseases. The program includes three sessions to help families prepare for future medical decisions and improve their quality of life. Researchers will compare …
Sponsor: Children's National Research Institute • Aim: Symptom relief
Last updated Jun 27, 2026 09:00 UTC
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Scientists track rare dystonia to map its genetic roots
Knowledge-focused OngoingThis study is observing up to 198 people with rapid-onset dystonia-parkinsonism (RDP) or related genetic mutations. Researchers aim to identify affected individuals, document how common the disease is, and track its progression over time. Participants undergo assessments of sympt…
Sponsor: State University of New York at Buffalo • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:29 UTC
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Global brain surgery matchmaker aims to help kids with rare movement disorders
Knowledge-focused By invitation onlyThis study is building an online platform called DBS MatchMaker to connect doctors around the world who treat rare movement disorders with deep brain stimulation (DBS). The goal is to help doctors share knowledge and find the best ways to treat patients. Up to 500 people of all a…
Sponsor: Boston Children's Hospital • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:06 UTC