Plain-English translation of NCT06393478 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a registry study—a long-term tracking program—that collects health information and heart test results from adults who have angina (chest pain) or similar symptoms and have undergone special heart tests to measure blood vessel function. The study is following people for up to 5 years to understand how their condition changes over time and what factors affect their health outcomes.
Many people have chest pain caused by problems with the small blood vessels in the heart, but we don't fully understand how these conditions develop or how to best treat them. This registry will help doctors learn more about these heart vessel problems and identify patterns that could improve care.
You likely qualify if…
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If you join, researchers will collect your basic health information, medical history, lab results, and details from your heart procedures at enrollment. Then you'll be checked on every 6 months for up to 5 years—either through office visits or phone calls with the research team—so they can track any heart problems you experience and monitor your medications and symptoms. Most of this information comes from your existing medical records, so there's minimal burden on you.
AI-generated summary from trial data · Jun 14, 2026 · Not medical advice
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