Clin2
NCT06552052Possibly a fitRecruiting

Natural history study of genetic blood vessel disease

Multisystemic Smooth Muscle Dysfunction SyndromeACTA2

Part of Genetic & congenital, Heart & circulation clinical trials.

This study tracks the health of people with a confirmed ACTA2 gene change over time to better understand the disease. It may help researchers learn how to improve care for this condition.

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

Phase
N/A
Enrollment
50 people
Ages
4 weeks and older
Study type
Observational

Who can take part

  • You have a confirmed change in the ACTA2 gene
  • Your medical records since birth are available
  • Both parents or legal guardians speak English and can give consent
  • You are able to travel to the study site
  • You are not pregnant

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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