Dystonia Genotype-Phenotype Correlation
NCT03428009
This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .
Summary
The purpose of this study is to (1) investigate the effect of known dystonia-causing mutations on brain structure and function, to (2) identify structural brain changes that differ between clinical phenotypes of dystonia, and to (3) collect DNA, detailed family history, and clinical phenotypes from patients with idiopathic dystonia with the goal of identifying new dystonia-related genes. Investigators will be recruiting both healthy control subjects and subjects with any form of dystonia.
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Dystonia
- Dystonia; Idiopathic
- Dystonia, Primary
- Dystonia, Secondary
- Dystonia, Familial
- Dystonia Disorder
- Dystonias, Sporadic
- Dystonia; Orofacial
- Dystonia Lenticularis
- Dystonia, Paroxysmal
- Dystonia 6
- Dystonia 5
- Dystonia 8
- Dystonia 9
- Dystonia 19
- Dystonia 10
- Dystonia 11
- Dystonia 20
- Dystonia 12
- Dystonia, Focal
- Dystonia of Head
- Dystonia, Diurnal
Eligibility basics and study details
- Study type
- Observational
- Phase
- Not applicable
- Ages
- 11 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Sponsor
- University of Texas Southwestern Medical Center
- Last updated on ClinicalTrials.gov
- September 23, 2026
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
Texas · 1
- University of Texas Southwestern Medical Center · Dallas, TX
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.