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NCT06512571Possibly a fitRecruiting

Heart changes in Fabry disease: an observational study

Fabry Disease, Cardiac Variant

Part of Brain & nervous system, Genetic & congenital, Heart & circulation, Kidney & urinary, Skin clinical trials.

This study looks at people with Fabry disease, a genetic condition that can cause the heart muscle to thicken. Researchers want to understand how the heart's blood vessels change over time, which may help improve care for Fabry disease.

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

Phase
N/A
Enrollment
300 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You are 18 years old or older.
  • Your heart ultrasound shows the thickest part of the heart muscle is 13 mm or more.
  • You have at least 2 warning signs of Fabry disease (like heart changes, skin growths, nerve pain, or family history).
  • Your thickened heart muscle is not due to another known cause (like high blood pressure).
  • You are willing to join the study and be followed for at least one year.

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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