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Arrhythmia Genetics in the NEtherlandS (AGNES)

A

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Status

Unknown

Conditions

Myocardial Infarction First
Ventricular Fibrillation

Study type

Observational

Funder types

Other

Identifiers

NCT03007199
CCMO # 13598

Details and patient eligibility

About

The AGNES case-control set consists of individuals with a first acute ST-elevation myocardial infarction. AGNES cases have ECG- registered ventricular fibrillation occurring before reperfusion therapy for an acute and first ST-elevation myocardial infarction. AGNES controls are individuals with a first acute ST-elevation myocardial infarction but without ventricular fibrillation. All cases and controls are recruited at seven heart centers in The Netherlands. The investigators' exclude individuals with an actual non-ST-elevation myocardial infarction, prior myocardial infarction, congenital heart defects, known structural heart disease, severe comorbidity, electrolyte disturbances, trauma at presentation, recent surgery, previous coronary artery bypass graft or use of class I and III antiarrhythmic drugs. Individuals who develop ventricular fibrillation during or after percutaneous coronary intervention are not eligible. Furthermore, because early reperfusion limits the opportunity of developing ventricular fibrillation, potential control subjects undergoing percutaneous coronary intervention within 2 h after onset of myocardial ischemia symptoms were not included. This time interval is based on the observation that >90% of cases develop ventricular fibrillation within 2 h after onset of the complaint of symptoms.

Enrollment

2,000 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. First ST elevation myocardial infarction (STEMI)
  2. Between 18 and 80 years old

Exclusion criteria

  1. A grandparent from non-European descent
  2. Inborn errors; congenital heart defects.
  3. Prior myocardial infarction (either STEMI or non-STEMI)
  4. Previous CABG (coronary artery bypass graft)
  5. Use of anti-arrhythmic drugs with the exception of beta-blockers, Ca2+-antagonists and lanoxin.
  6. Severe current co morbidity (electrolyte disturbances, K+>5.5, K+<3.0 mmol/L, anaemia, trauma, surgery).

Trial design

2,000 participants in 2 patient groups

AGNES Controls
Description:
AGNES controls are individuals with a first acute ST-elevation myocardial infarction but without ventricular fibrillation.
AGNES cases
Description:
AGNES cases have ECG- registered ventricular fibrillation occurring before reperfusion therapy for an acute and first ST-elevation myocardial infarction.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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