Plain-English translation of NCT03412435 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a research registry — a large database — that collects information from people diagnosed with acute myocardial infarction (a heart attack). Researchers will gather data from 5,000 patients, some looking back at past medical records and some enrolling new patients going forward. The goal is to understand how different treatments work for heart attack patients.
Heart attacks are serious and life-threatening, and doctors use several different treatment approaches — medications, procedures to open blocked arteries, or surgery. This registry will help researchers learn which treatments work best for different patients and how to improve outcomes for people who have had a heart attack.
You likely qualify if…
You likely don't qualify if…
Some participants will be enrolled by sharing their existing medical records from their heart attack treatment (retrospective data). Others will enroll going forward and have their medical information collected as part of the registry over time. There is no new medication or procedure required — this is purely a data collection study where your treatment records will be added to the database to help advance heart attack research.
AI-generated summary from trial data · Jun 11, 2026 · Not medical advice
South Korea
CardioVascular Research Foundation, Korea
Enrollment target
~5,000 participants
Started
April 2018
Primary completion
December 2026
Age range
19 Years and older
Last updated on clinicaltrials.gov in January 2026.
Reach out to the team running this trial. Response times vary — some teams are faster than others.
Central contact
Seung-jung Park, MD
Seung-Jung Park
Tell us you're interested and we'll help connect you with the research team. We'll walk you through what to expect first — no email needed to get started.