- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02895425
Registry for End Stage Renal Failure (REIN)
September 8, 2016 updated by: Centre Hospitalier de Cayenne
Réseau, Epidémiologie, Information, Néphrologie (Network Epidemiology Information Nephrology)
The rein registry collects case record data from patients with end stage renal disease followed in French Guiana.
This allows to generate incidence and rates for terminal renal disease, mortality rates for each territory.
The regional data are pooled in order to get national statistics for end stage renal disease and transplantation activity in order to adapt prevention to the main causes of renal failure and treatment and care infrastructure.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
1000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
French Guiana
-
Cayenne, French Guiana, France, 97306
- Recruiting
- General Hospital of Cayenne
-
Contact:
- Mathieu Nacher, MD, PhD
- Phone Number: 5024 0594395024
- Email: mathieu.nacher@ch-cayenne.fr
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patient with End Stage Renal Failure followed in one of the dialisys sites in frnech Guiana
Description
Inclusion Criteria:
- End Stage Renal Failure
Exclusion Criteria:
- Refusal to participate
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Death
Time Frame: 10 years
|
10 years
|
Transplant
Time Frame: 10 years
|
10 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2011
Primary Completion (Actual)
January 1, 2011
Study Completion (Anticipated)
January 1, 2021
Study Registration Dates
First Submitted
September 6, 2016
First Submitted That Met QC Criteria
September 8, 2016
First Posted (Estimate)
September 9, 2016
Study Record Updates
Last Update Posted (Estimate)
September 9, 2016
Last Update Submitted That Met QC Criteria
September 8, 2016
Last Verified
September 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REIN
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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