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Primary ventricular fibrillation and sudden death during a first myocardial infarction: Genetic basis

Assessment of genetic predisposition to development of primary ventricular fibrillation in patients with acute myocardial infarction

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN11980212
Enrollment
4000
Registered
2016-12-29
Start date
2009-09-01
Completion date
Unknown
Last updated
2021-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myocardial infarction Circulatory System Myocardial infarction

Interventions

Following provision of informed consent, all participants have a blood sample taken which is immediately frozen for the future primary outcome analysis. Peripheral blood samples are drawn into n°3 BD

Sponsors

Università degli Studi di Pavia
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Cases: 1. Age between 18 and 75 years, inclusive 2. At least one episode of cardiac arrest due to ventricular fibrillation within 24 h of onset of symptoms of heart attack documented in the index electrocardiogram Controls: 1. Age between 18 and 75 years, inclusive 2. Episode of myocardial infarction within 24 h of onset of symptoms

Exclusion criteria

Exclusion criteria: Case Patients Exclusion criteria: 1. Age younger than 18 or older than 75 years 2. History of previous myocardial infarction 3. Pre-existing significant cardiac disease and / or associated with Ejection Fraction less than or equal to 30% 4. Presence of arrhythmogenic diseases that affect the occurrence of major ventricular arrhythmias (TV, FV) independently by the ischemic event (arrhythmogenic right end/or left ventricular cardiomiopathies, long- and short-QT syndrome; Brugada syndrome and Cathecolaminergic polymorphic ventricular tachicardia) Control Patients Exclusion criteria: 1. Age younger than 18 or older than 75 years 2. History of previous myocardial infarction 3. Pre-existing significant cardiac disease and / or associated with Ejection Fraction less than or equal to 30% 4. Presence of arrhythmogenic diseases that affect the occurrence of major ventricular arrhythmias (TV, FV) independently by the ischemic event (arrhythmogenic right end/or left ventricular cardiomiopathies, long- and short-QT syndrome; Brugada syndrome and Cathecolaminergic polymorphic ventricular tachicardia)

Design outcomes

Primary

MeasureTime frame
Genetic loci associated with ventricular fibrillation risk during myocardial infarction are assessed through analysis of 1,536 SNPs (single nucleotide polymorphisms) using the GoldenGate method (Illumina) with a custom-made chip and the Genome Wide Association Study (GWAS) technique at 1 year.

Secondary

MeasureTime frame
1. Relationship between the occurrence of ventricular fibrillation and 1.1. familiarity for sudden death 1.2. Smoking habit 1.3. Hypokalemia 1.4. Hyperkalemia 1.5. Prolonged corrected QT interval is assessed using information collected using case reports collected at baseline 2. Survival status is assessed through medical record review at one year

Countries

Italy

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026