Plain-English translation of NCT04160533 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a registry study — a large database that collects medical information from thousands of patients with high blood pressure. Doctors and researchers will use this information to understand the different ways high blood pressure affects people and to develop more personalized treatment plans. The study is recruiting over 10,000 participants from primary care clinics.
High blood pressure affects millions of people, but it doesn't affect everyone the same way. By collecting detailed medical records from many patients, researchers hope to identify different patterns and causes of high blood pressure so that treatments can be tailored to each person's specific needs rather than using a one-size-fits-all approach.
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You would sign a consent form giving permission for your existing medical records to be entered into a secure, confidential database. Your doctor or clinic staff would upload your examination results and treatment information into the registry through a secure online system — no extra visits or procedures are needed. Your data would be coded to protect your privacy and shared with the research team only through encrypted, secure channels.
AI-generated summary from trial data · Jun 19, 2026 · Not medical advice
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