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Hereditary Thrombophilia in the Pathogenesis of Myocardial Infarction and Coronary Artery Bypass Graft Occlusion: New Role for an Old Actress.

Hereditary Thrombophilia in the Pathogenesis of Myocardial Infarction and Coronary Artery Bypass Graft Occlusion: New Role for an Old Actress. - HERITAGE-ACS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON42575
Enrollment
887
Registered
2016-01-26
Start date
2016-03-14
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

acute coronary syndrome Heart attack

Interventions

None listed

Sponsors

Sint Antonius Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with unstable angina or non-ST-segment elevation myocardial infarction. Age above 18 years;ST-segment elevation myocardial infarction (STEMI) patients for comparison will be selected from an existing dataset of ongoing trial (i.e., POPular Genetics).

Exclusion criteria

Exclusion criteria: Patients who are unable or unwilling to give informed consent (e.g., due to metal illnesses or inability to understand Dutch language). Individuals younger than 18 years of age. Patients with previous ST-segment elevation myocardial infarction (STEMI)

Design outcomes

Primary

MeasureTime frame
Prevalence of factor V Leiden or Prothrombin G20210A in STEMI as compared to NSTEMI/uAP patients.

Secondary

MeasureTime frame
Hemorrhagic complications during the index hospitalization in patients with versus without factor V Leiden or prothrombin G20210A mutations.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)