Clin2
NCT03322306Possibly a fitEnrolling by invitation

Genetic testing study for inherited neurological conditions

Neuro-Degenerative Disease

Part of Brain & nervous system, Genetic & congenital clinical trials.

This trial looks for genetic causes of inherited (in family) neurological diseases by using genetic screening. If you might have an inherited neurological condition, this study may help explain why symptoms happen and guide future care.

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

Phase
N/A
Enrollment
200 people
Ages
18 years to 80 years
Study type
Observational

Who can take part

  • Be age 18 or older (or your legal guardian can join for consent)
  • Have a suspected inherited neurological disease (runs in the family or seems genetic)
  • Be able to give informed consent (or your guardian can)
  • Not be allergic to local numbing medicines used for skin procedures
  • Be healthy enough to tolerate a skin biopsy (a small skin sample)
  • Not have a bleeding problem history, and avoid blood thinners/anticoagulants; NSAID pain medicines may need to be stopped before the biopsy

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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