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Recruiting Observational

French Renal Epidemiology and Information Network (REIN) Registry

NCT03967808 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2001-01
Last updated
2021-07-28

Condition(s) studied

End-stage Renal Disease

Study summary

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.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
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

Primary outcome measure(s)

  • Occurence of end stage renal disease in Renal Replacement therapy — One year
    New (incident) patients are reported from the first day of Renal Replacement Therapy - either dialysis or renal transplantation

Trial sites (1)

FacilityCityRegionStatus
Nephrology unit, University hospital Nancy France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03967808 on ClinicalTrials.gov ↗ ← All trials in France