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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
Rachel C Myles, MBBS, PhD
0141 451 6121
Rachel.Myles@glasgow.ac.uk
Caroline J Coats, MBBS, PhD
0141 451 6121
Caroline.Coats@glasgow.ac.uk
Cardiomyopathies Genetic Predisposition to Disease
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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.
Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.
The recruitment start and end dates are as follows:
You can take part if:
You may not be able to take part if:
This is in the inclusion criteria above
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Rachel C Myles, MBBS, PhD
0141 451 6121
Rachel.Myles@glasgow.ac.uk
Caroline J Coats, MBBS, PhD
0141 451 6121
Caroline.Coats@glasgow.ac.uk
The study is sponsored by NHS Greater Glasgow and Clyde and is in collaboration with University of Glasgow; Roche Diagnostics GmbH.
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
You can print or share the study information with your GP/healthcare provider or contact the research team directly.
