French Renal Epidemiology and Information Network (REIN) Registry
Condition(s) studied
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| Nephrology unit, University hospital | Nancy | France | Recruiting |
More Central Hospital, Nancy, France trials in France
Other trials for the same condition
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