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Armenian National Registry of Myocardial Infarction

Armenian National Registry of ST-elevation Myocardial Infarction,a Multicenter Prospective Observational Study With Biocollection

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06048003
Acronym
ARMI
Enrollment
2500
Registered
2023-09-21
Start date
2023-12-01
Completion date
2025-12-30
Last updated
2023-12-26

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

Conditions

ST Elevation Myocardial Infarction

Keywords

STEMI, Myocardial infarction, acute coronary syndrome, CV mortality, biobanking

Brief summary

This is a national, multicenter prospective observational study of patients presenting to hospitals in Armenia with STEMI diagnosis. The main questions it aims to answer are: * Determine the rate of in-hospital mortality for the patients with STEMI admitted to the participating hospitals. * Compare short and long-term CV and all-cause mortality and hospitalization. * Determine how professional guidelines are followed in real-world situations.

Detailed description

Although the state program on primary percutaneous coronary intervention in ST elevated myocardial infarction, which was launched in 2015 helped to drastically decrease STEMI mortality rates, patients who had survived usually develop heart failure (HF) which leads to increased economic burden for the Armenian healthcare system. The total duration of the study will be 24 months. The target number of the inclusion is 2500 patients. The follow-up period for enrolled patients will be 12 months.

Interventions

No specific intervention

Sponsors

Santé Arménie French-Armenian Research Center
CollaboratorOTHER
Armenian Cardiologists Association
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Adult patient (≥ 18 years of age), 2. Admitted to the participating centers for a STEMI within 48 hours of symptom onset: characterized by a rise and fall of cardiac markers (troponins) together with ST elevation in at least two contagious leads or LBBB. 3. Have given signed informed consent to participate in the study. Non-Inclusion Criteria: 1. MI occurring ≤ 48 hours after PCI or CABG 2. The patient or the legal representative refused to sign the informed consent

Exclusion criteria

Withdrawal of the informed consent

Design outcomes

Primary

MeasureTime frameDescription
Rate of the in-hospital mortalityDuring 5 to 7 days of hospitalizationDetermine the rate of the in-hospital mortality for the patients with STEMI admitted to the participating hospitals

Secondary

MeasureTime frameDescription
Cardiovascular mortality30 days and 12 monthsCompare short-term (30 days) and long-term (12 months) CV mortality depending on the management strategies.
All-cause mortality30 days and 12 monthsCompare short-term (30 days) and long-term (12 months) all-cause mortality.

Countries

Armenia

Contacts

Primary ContactHamlet G Hayrapetyan, Prof.
cardioerebouni@yahoo.com+37493555050
Backup ContactHripsime V Poghosyan, Dr.
hripsime.poghosyan@santearmenie.org+37477234994

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026