Imaging Genetics of Laryngeal Dystonia Study

This observational study is looking at the relationship between brain changes and genetic factors in people with laryngeal dystonia (also called spasmodic dysphonia). Researchers will use MRI scans (magnetic resonance imaging, a way to look inside the body) of the brain and collect blood samples for genetic studies. They hope to identify brain markers that can help tell the difference between different types of laryngeal dystonia, predict its development, and confirm related gene mutations. You may be able to join if you have laryngeal dystonia (adductor or abductor, familial or sporadic), voice tremor (essential or dystonic), or muscle tension dysphonia. The study aims to enroll 410 participants, but its current status is unclear.

Study design
This is an observational study with a planned enrollment of 410 participants. It is not a treatment study and does not involve different treatment groups.
What's involved
You would undergo functional and structural MRI scans of your brain and have blood samples collected for genetic studies.
Compensation
Not stated in the trial record.
Follow-up
Brain changes in laryngeal dystonia will be measured at 5 years.

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NCT03042975

Imaging Genetics of Laryngeal Dystonia

Recruiting
Not specifiedAll AgesObservational
Kristina Simonyan
~410 participants
Updated 2025-12-02 on ClinicalTrials.gov
What's tested:MRIBlood draw

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Brain changes in laryngeal dystonia
Measured over 5 years
Laryngeal Dystonia
Unaffected Relatives of Laryngeal Dystonia Patients
Voice Tremor
Muscle Tension Dysphonia
1 sites across 1 states
Massachusetts1
  • Kristina Simonyan, MD, PhD · PRINCIPAL_INVESTIGATOR · Massachusetts Eye and Ear Infirmary

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Eligibility criteria

Inclusion

phenotype: adductor or abductor
genotype: familial or sporadic 3. Voice Tremor patients
essential or
dystonic 4. Muscle tension dysphonia patients 5. Unaffected relatives of laryngeal dystonia patients with
familial laryngeal dystonia
early-onset laryngeal dystonia (onset at ≤ 35 y.o.)
typical onset laryngeal dystonia (onset at ≥ 40 y.o.) 6. Native English speakers. 7. Right-handedness. 8. Normal cognitive status.
  • Brain changes in laryngeal dystonia5 years

    Identify imaging biomarker of laryngeal dystonia