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NCT06548555Completed

A Study to Evaluate the Impact of Long-term Digital Education vs Standard of Care on LDL-C Levels in Post Myocardial Infarction Patients

A Prospective Multicentric Study to Evaluate the Impact of Long-term Digital Education vs Standard of Care on LDL-C Levels in Post Myocardial Infarction Patients in the Czech Republic

Source: ClinicalTrials.gov · Last updated 4 Jun 2026

Brief summary (registry, in English)

The purpose of this study was to demonstrate the impact of digital education on the cardiovascular risk factors in post-Myocardial Infarction patients and to generate evidence for broad implementation of the proposed education program.

Status (registry)
Completed
Study type
Observational
Enrollment
121 (actual)
First submitted
7 Aug 2024
Start date
8 Mar 2023
Primary completion date
24 Oct 2024
Lead sponsor
Novartis Pharmaceuticals
NCT number
NCT06548555

What you commit to

  • Study type: Observational
  • Participants enrolled: 121
  • From 8 Mar 2023 to the primary completion date, 24 Oct 2024
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of previous myocardial infarction,
  • History of previous coronary intervention due to ASCVD (percutaneous coronary intervention (PCI) or coronary artery bypass graft (CABG)),
  • Patients treated with inclisiran prior to the hospitalization for myocardial infarction.

Other illness

  • History of ischemic stroke,
  • Any surgical or medical condition, which in the opinion of the investigator, may place the participant at higher risk from his/her participation in the study, or is likely to prevent the participant from complying with the requirements of the study or completing the study,

Other

  • Participants meeting any of the following criteria are not eligible for inclusion in this study:
  • Patients diagnosed with homozygous familial hypercholesterolemia,
  • Unwillingness or inability (e.g., physical, or cognitive) to comply with study procedures (including adherence to study visits and fasting blood draws) and schedule,
  • Participation in any other interventional study, both treatment and non-treatment interventional study,

Who the study is looking for

  • Participants eligible for inclusion in this study must fulfil all the following criteria:
  • Male or female patients ≥18 years of age,
  • At the Screening Visit, participants must be hospitalized for the first myocardial infarction. This must be a spontaneous MI (either ST-elevation MI or non-ST-elevation MI), which was not the result of percutaneous coronary intervention (PCI) or coronary artery bypass graft (CABG). Confirmation of MI is a combination of signs or symptoms consistent with presentation of MI, and at least one of the following (adapted from (Thygesen, et al., 2018)):
    • Documentation of cardiac biomarkers that exceed the diagnostic threshold of a local laboratory for MI
    • Pathological Q waves on ECG or other ECG changes as defined in Appendix 2
    • Imaging evidence of loss of viable myocardium or regional wall motion abnormality in a pattern consistent with an infarction or ischemic etiology
    • Identification of a coronary thrombus by angiography at the time of presentation with MI,
  • LDL-C ≥ 1.8 mmol/L at the time of the hospitalization,
  • Ability to participate in the hybrid educational program (must be able to receive emails and watch online educational videos),
  • Patients must provide written consent to participate in the study.

Age in the registry: 18 years to 90 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
-
Coordinator of this site? Confirm its status
Brno-BohuniceCzechiaUnknown status
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Coordinator of this site? Confirm its status
České BudějoviceCzechiaUnknown status
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Coordinator of this site? Confirm its status
Ostrava-PorubaCzechiaUnknown status
-
Coordinator of this site? Confirm its status
PragueCzechiaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.