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NCT06701851Possibly a fitRecruiting

Brain study for movement disorder with PRRT2 gene change

Paroxysmal Dyskinesia

Part of Brain & nervous system clinical trials.

This study uses brain scans to understand movement problems in people with a specific genetic change (PRRT2) that causes sudden, brief episodes of uncontrolled movements. It may help researchers find better ways to treat this condition.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
1 people
Ages
18 years to 75 years
Study type
Interventional

Who can take part

  • You have a movement disorder called paroxysmal kinesigenic dyskinesia (sudden, brief episodes of uncontrolled movements) caused by a change in the PRRT2 gene.
  • You are between 18 and 75 years old.
  • You are able to control these movement episodes during the study.
  • You live in France and have health insurance.
  • You do not have any metal in your body that would make an MRI unsafe (for example, pacemaker, metal clips, or certain implants).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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