Plain-English translation of NCT06521801 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a research registry—a large database where doctors collect information about patients with kidney disease, heart disease, or both conditions together. Researchers will study this real-world information to better understand how these diseases interact and what treatments work best for people who have both.
People with kidney disease have a much higher risk of heart disease and heart attacks, but doctors often don't treat them as aggressively as they should because they worry about medication side effects. This registry exists to gather real-world information so doctors can make better, safer treatment decisions for patients with both conditions.
You likely qualify if…
You likely don't qualify if…
Your participation is automatic—you'll be enrolled through your kidney or cardiology clinic at Barts Health without needing to sign a separate consent form. Your medical records, test results, and health information will be added to a secure research database. There are no additional visits or procedures required beyond your regular medical care.
AI-generated summary from trial data · Jun 1, 2026 · Not medical advice
United Kingdom
~60,000 participants
Started
August 2024
Primary completion
June 2030
Age range
16 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
Krishnaraj Rathod, MBBS, PhD
Queen Mary University of London
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.