Clin2
NCT06446271Likely a fitRecruiting

Biomarkers in Scottish Cardiomyopathy Registry

CardiomyopathiesGenetic PredispositionCardiomyopathy, Primary

Part of Heart & circulation clinical trials.

This study looks for signs of heart muscle disease (cardiomyopathy) in people who have certain genetic changes. It aims to find better ways to monitor and treat the condition.

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

Phase
N/A
Enrollment
750 people
Ages
10 years and older
Study type
Observational

Who can take part

  • You are 10 years old or older.
  • You have a genetic change (mutation) in a gene linked to cardiomyopathy, or are being tested for one.
  • You can travel to the study centre in Scotland for appointments.
  • You do not have a life-threatening illness that would make it hard to complete the study.
  • You are not currently in a blinded drug trial.

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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