Clin2
NCT05354622Possibly a fitRecruiting

Genetic testing study for inherited leg stiffness

Hereditary Spastic ParaplegiaNeurodegenerative DiseasesPediatric DisorderSpasticity, MuscleMotor Neuron DiseaseMovement Disorders

Part of Bones, joints & muscles, Brain & nervous system, Genetic & congenital, Mental health clinical trials.

This study looks at genes (DNA) to understand an inherited condition that causes gradually worsening leg stiffness. It may help researchers learn what causes the condition and potentially guide future care.

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

Phase
N/A
Enrollment
200 people
Ages
1 month to 30 years
Study type
Observational

Who can take part

  • You have a clinical diagnosis of progressive spasticity (getting stiffer over time).
  • Your symptoms mainly involve stiffness/spasms that are worsening.
  • You may need to provide a sample for genetic testing (DNA testing).
  • You may need to share your medical and family history to interpret results.

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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