The Multicenter Cardiology Monitoring Platform Registry

Recruiting now

Conditions studied: Heart Failure, Cardiomyopathies, Atrial Fibrillation, Ventricular Arrythmia, Coronary Artery Disease, Ventricular Tachycardia

In brief

The multicenter Cardiology Monitoring Platform registry (mCMP-registry) is a prospective observational registry including multi-omics (diagnostic) measurements performed as part of routine clinical care, bio-banking (optional), and yearly questionnaires (optional). It's objective is to optimize (early) diagnosis and risk-stratification of (early) cardiovascular diseases, specifically cardiomyopathy phenotypes, arrhythmias, and coronary artery disease, and to create a better understanding of underlying pathophysiological processes.

Key facts

Study ID

NCT04976348

Run by

Maastricht University Medical Center

People needed

40000

Starts

2021-07-01

Expected to finish

2051-12-01

Last updated by the study team

2024-11-21

Who can join

Age: 16 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Referred to the cardiology or genetic department for heart failure like symptoms (as stated in the ESC 2016 Guidelines(3)) or for cardiac/cardiogenetic screening;
• Age ≥16 years.

You may not qualify if…

• Unwillingness to participate or unable to give written informed consent (e.g. due to language barriers or severe intellectual disability).

Where it is running

• Maastricht UMC+ — Maastricht, Limburg, Netherlands (enrolling)

Full record on ClinicalTrials.gov

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