Clinical Trial

French Renal Epidemiology and Information Network (REIN) Registry

Study acronym: REIN-LOR
Recruiting
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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.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2019-05-27; most recent amendment 2021-07-27.
Trial Details
NCT Number NCT03967808
Lead Sponsor Central Hospital, Nancy, France
Collaborators: Agence de La Biomédecine
Conditions End-stage Renal Disease
Enrollment 6,000 participants
Start Date 2001-01
Primary Completion 2050-12 (estimated)
Study Completion 2050-12 (estimated)
Updated on ClinicalTrials.gov 2021-07-28