French Renal Epidemiology and Information Network (REIN) Registry
Sponsored by Central Hospital, Nancy, France
About this trial
Last updated 4 years ago
Study ID
REIN-01
Status
Recruiting
Type
Observational [Patient Registry]
Placebo
No
Accepting
All
All
Not accepting
Healthy Volunteers
Trial Timing
Started 24 years ago
What is this trial about?
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.
What are the participation requirements?
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
Locations
Location
Status
Recruiting