French Renal Epidemiology and Information Network (REIN) Registry
REIN-LOR
1 other identifier
observational
6,000
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2001
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2001
CompletedFirst Submitted
Initial submission to the registry
May 27, 2019
CompletedFirst Posted
Study publicly available on registry
May 30, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2050
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2050
July 28, 2021
July 1, 2021
49.9 years
May 27, 2019
July 27, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Occurence of end stage renal disease in Renal Replacement therapy
New (incident) patients are reported from the first day of Renal Replacement Therapy - either dialysis or renal transplantation
One year
Eligibility Criteria
All new patients reaching end-stage chronic renal failure and requiring support by a renal replacement therapy
You may qualify if:
- All patients with end stage renal disease on renal replacement therapy
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Central Hospital, Nancy, Francelead
- Agence de La Biomédecinecollaborator
Study Sites (1)
Nephrology unit, University hospital
Nancy, 54000, France
Related Publications (2)
Lassalle M, Ayav C, Frimat L, Jacquelinet C, Couchoud C; Au Nom du Registre REIN. The essential of 2012 results from the French Renal Epidemiology and Information Network (REIN) ESRD registry. Nephrol Ther. 2015 Apr;11(2):78-87. doi: 10.1016/j.nephro.2014.08.002. Epub 2014 Nov 1.
PMID: 25457107BACKGROUNDCouchoud C, Stengel B, Landais P, Aldigier JC, de Cornelissen F, Dabot C, Maheut H, Joyeux V, Kessler M, Labeeuw M, Isnard H, Jacquelinet C. The renal epidemiology and information network (REIN): a new registry for end-stage renal disease in France. Nephrol Dial Transplant. 2006 Feb;21(2):411-8. doi: 10.1093/ndt/gfi198. Epub 2005 Oct 18.
PMID: 16234286BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Emmanuelle Laurain, MD
Central Hospital, Nancy, France
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 30 Years
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Doctor
Study Record Dates
First Submitted
May 27, 2019
First Posted
May 30, 2019
Study Start
January 1, 2001
Primary Completion (Estimated)
December 1, 2050
Study Completion (Estimated)
December 1, 2050
Last Updated
July 28, 2021
Record last verified: 2021-07