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French Renal Epidemiology and Information Network (REIN) Registry

NCT03967808 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 6000

Last updated 2021-07-28

No results posted yet for this study

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.

Conditions

  • End-stage Renal Disease

Sponsors & Collaborators

  • Agence de La Biomédecine

    collaborator OTHER_GOV

  • Central Hospital, Nancy, France

    lead OTHER

Principal Investigators

  • Emmanuelle Laurain, MD · Central Hospital, Nancy, France

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-01-31
Primary Completion
2050-12-31
Completion
2050-12-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03967808 on ClinicalTrials.gov