Plain-English translation of NCT06512493 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Read our Coronary Artery Disease research guide →This is a large registry—essentially a medical database—that collects information from patients who have had a procedure called percutaneous coronary intervention (PCI) to treat blocked heart arteries. The registry gathers details about your health, the procedure you received, and how you're doing afterward, so that hospitals can track treatment quality and help doctors make better decisions about your care.
After heart artery procedures, patients still face risks of future heart problems because the underlying disease can continue to progress. Doctors need to personalize treatment—choosing the right blood-thinning medications, managing cholesterol, and controlling other risk factors—but this is complicated. By collecting real-world information from many patients, this registry helps hospitals and doctors understand what works best and identify patients who may need extra support or different treatment approaches.
You likely qualify if…
You likely don't qualify if…
You would allow the hospital to share your medical information—including details about your diagnosis, the procedure you received, your medications, and your health outcomes over time—with the registry. The study collects this information from your existing medical records and follow-up visits; you are not required to do anything extra beyond your normal heart care appointments. The registry then uses this information to give hospitals feedback on how well they are treating patients and to help improve care quality.
AI-generated summary from trial data · Jun 11, 2026 · Not medical advice
Netherlands