Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH)

Recruiting now

Conditions studied: Cardiomyopathies, Genetic Predisposition, Cardiomyopathy, Primary

In brief

Genetic cardiomyopathy is increasingly recognised and can lead to heart failure, arrhythmia and sudden cardiac death. Some gene positive patients have rapidly progressive disease with high rates of heart failure and cardiac transplantation, while others present with SCD. Other gene positive patients will never develop cardiomyopathy. At present, we cannot distinguish between these groups and rely on expensive and labour-intensive surveillance by electrocardiography, echocardiography and sometimes cardiac magnetic resonance imaging. This study will investigate existing and novel biomarkers (including blood, urine electrocardiographic and imaging) at various stages of disease in patients with a personal or family history of TTN, MYBPC3, LMNA, FLNC or DSP gene variant, which are known to cause cardiomyopathy.

Key facts

Study ID

NCT06446271

Run by

NHS Greater Glasgow and Clyde

People needed

750

Starts

2024-06-26

Expected to finish

2027-03-19

Last updated by the study team

2024-07-03

Who can join

Age: 10 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female ≥10 years of age
• Written informed consent / assent
• Pathogenic or likely pathogenic variant in a cardiomyopathy gene (TTN, LMNA, MYBPC3, DSP, FLNC) or undergoing predictive genetic testing (if negative these people would be invited to enter the control arm)

You may not qualify if…

• Unable to consent.
• Geographical / social reasons preventing attending study centre
• Unable to complete study assessments.
• Severe non-cardiac disease expected to reduce life expectancy < 5 years
• Current participation in a blinded drug interventional trial (or treatment within 4 weeks)

Where it is running

• Queen Elizabeth University Hospital — Glasgow, United Kingdom (enrolling)

Full record on ClinicalTrials.gov

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