French Renal Epidemiology and Information Network (REIN) Registry
Recruiting · NCT03967808 · Observational (researchers observe without assigning treatment) · Lead sponsor: Central Hospital, Nancy, France
View the official record on ClinicalTrials.gov →What this trial is 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.
Who can take part
Age range
No age limits stated
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
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
Where it is running
1 location listed.
- Nephrology unit, University hospital - Nancy, France