Registry for people with kidney failure on dialysis or similar treatment
Part of Kidney & urinary, Women’s health & pregnancy clinical trials.
This study is a kidney disease registry that collects information from people with end-stage kidney failure who are receiving ongoing kidney replacement treatment. It may help doctors better understand kidney disease over time and improve care planning.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have end-stage kidney disease
- You are receiving kidney replacement therapy (such as dialysis or a similar treatment)
- You are not in a short-term kidney problem expected to improve within about 45 days
- You are willing to participate (you have not refused)
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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This is an observational registry that collects information from people with kidney disease who are seen by the kidney team at Royal London Hospital. It helps researchers study heart and kidney health over time without needing extra tests or visits.
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This study looks at real-world information about people living with advanced chronic kidney disease. Your participation mainly involves allowing researchers to use your existing medical data to understand care and outcomes.
This study is collecting information from people with chronic kidney disease (CKD) to understand how the disease progresses over time. It does not test any new treatments, so you keep your usual care.
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This trial is for people with a primary (main) kidney disease who can regularly see a kidney doctor. It sets up and includes patients for possible interventional (active) research studies, which may help improve kidney care for future patients.
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