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French Renal Epidemiology and Information Network (REIN) Registry

Recruitingn/aAges any - anyAllCentral Hospital, Nancy, France
NCT03967808 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The Renal Epidemiology and Information Network (REIN) Registry was created in 2002 (after study pilot in 2001) to contribute to the development and evaluation of health strategies aiming at improving prevention and management of end-stage renal disease, and promoting clinical and epidemiological research in this field. It relies on a network of nephrologists, epidemiologists, patients and public health representatives, coordinated regionally and nationally.

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📋 Eligibility rules (as published)
Inclusion Criteria: * All patients with end stage renal disease on renal replacement therapy Exclusion Criteria: * Patients with acute renal failure ( i.e. those who recover all or some renal function within 45 days or are considered as such by experts when they die before 45 days) * Patient's refusal
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What it tests

  • Not listed
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Where

1 site
Nephrology unit, University hospital
Nancy, France
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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