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End Stage Renal FailureREINNCT02895425

Registry for End Stage Renal Failure

An observational study of End Stage Renal Failure, run by Centre Hospitalier de Cayenne at 1 site in France.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Any age
Conditions the study is for
End Stage Renal Failure
How many people
1,000 participants
Where
1 siteFrance
Study dates
Jan 2011to Jan 2021
How long will I take part?
10 Years
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Patient with End Stage Renal Failure followed in one of the dialisys sites in frnech Guiana

Who may be able to join

  • End Stage Renal Failure

Who cannot join

  • Refusal to participate

Trial locations and contacts

1 site in 1 country.

France1 site, 1 recruiting
  • General Hospital of Cayenne

    Cayenne, French Guiana, 97306

    Mathieu Nacher, MD, PhD, 0594395024 ext. 5024, mathieu.nacher@ch-cayenne.fr

    Recruiting

Other trials in France

About this study

Official title: 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.

Being tested
Registry (No intervention)
Keywords
Renal Transplant
Medical subject headings
Renal Insufficiency, Chronic

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Registry (No intervention)Other

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Death

    Measured: 10 years

  2. Transplant

    Measured: 10 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Sep 2016 (estimated)
  2. Study startJan 2011
  3. Primary completionJan 2011
  4. Study completionJan 2021 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
1,000 participants (estimated)
Target duration
10 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT02895425
Sponsor's protocol ID
REIN
Acronym
REIN
Status last verified
Sep 2016
First submitted
6 Sep 2016
Last updated
9 Sep 2016
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of End Stage Renal Failure, run by Centre Hospitalier de Cayenne at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 9 Sep 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Death (time frame: 10 years). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Sep 2016.

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