French Renal Epidemiology and Information Network (REIN) Registry

Recruiting now

Conditions studied: End-stage Renal Disease

In brief

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.

Key facts

Study ID

NCT03967808

Run by

Central Hospital, Nancy, France

People needed

6000

Starts

2001-01-01

Expected to finish

2050-12-01

Last updated by the study team

2021-07-28

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

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

Where it is running

• Nephrology unit, University hospital — Nancy, France (enrolling)

Full record on ClinicalTrials.gov

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