Clin2
NCT02998710Possibly a fitRecruiting

Natural history study for homocystinuria due to CBS deficiency

Homocystinuria Due to CBS Deficiency

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

This study mainly observes what happens in people with homocystinuria caused by a CBS gene deficiency over time. It helps doctors better understand the condition’s natural course and may guide future treatments.

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

Phase
N/A
Enrollment
150 people
Ages
1 year to 65 years
Study type
Observational

Who can take part

  • You have a clinical diagnosis of homocystinuria (an imbalance of certain blood chemicals).
  • Your age is between 1 and 65 years.
  • You (or your child, if applicable) can give consent/assent to join the study.
  • You’re able and willing to follow study visits and procedures.
  • In the past 6 months, you did not take an experimental treatment for homocystinuria.

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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