Renal Insufficiency Clinical Trial
— VIgIEOfficial title:
Factors Related to Geographical Variation in the Incidence of End-stage Renal Failure: An Analysis in 5 French Regions
Verified date | July 2016 |
Source | Centre Hospitalier Universitaire de Besancon |
Contact | n/a |
Is FDA regulated | No |
Health authority | France: Ministry of Health |
Study type | Observational |
The REIN registry highlights significant disparities in the incidence of end-stage renal
disease (ESRD) between regions, especially in the North East of France. According to the
literature, the incidence of ESRD in an area could be related to contextual factors
influencing the needs for dialysis or transplantation (age structure, prevalence of risk
factors, socioeconomic and morbidity levels), as well as to primary and secondary care
provision (general practitioners and nephrologists) and to practice patterns in nephrology.
The aims of this project are the following:
1. to compare the incidence of renal replacement therapy (dialysis or preemptive
transplantation) for ESRD between the "départements" and the "cantons" belonging to the
5 regions of Eastern France (Alsace, Lorraine, Champagne-Ardenne, Bourgogne and
Franche-Comté), while taking into account differences in population sizes and spatial
patterns of the data,
2. to analyse the relations between incidence disparities and socioeconomic environment,
geographic accessibility to primary and secondary care and medical practice patterns,
after adjusting for morbidity and mortality rates (incidence of diabetes,
cardiovascular mortality).
This project will enable a better understanding of the mechanisms involved in the spatial
variations of ESRD incidence, while disentangling effects related to the need from effects
related to service supply in different socio-economic contexts. It will be possible to
identify a lack of equity in access to renal replacement therapy if, after adjusting for
need indicators, there were variations of incidence of ESRD related to availability of
service or to socioeconomic context. Highlighting such effects would lead to search for
corrective measures in collaboration with the different stakeholders.
Status | Completed |
Enrollment | 6835 |
Est. completion date | June 2016 |
Est. primary completion date | June 2016 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Age 18 and older - Resident of the 5 French administrative regions (Alsace, Bourgogne, Champagne-Ardenne, Franche-Comté, and Lorraine) - First renal replacement therapy by renal dialysis or preemptive kidney transplant between January 1st, 2010 and December 31, 2014 - Found in the REIN registry Exclusion Criteria: - Transfer from another French administrative region - Return to renal dialysis after graft rejection or a period without dialysis |
Observational Model: Ecologic or Community, Time Perspective: Retrospective
Country | Name | City | State |
---|---|---|---|
France | Centre d'Investigation Clinique, CHU de Besançon | Besançon | |
France | Hôpital William Morey, Néphrologie | Chalon sur Saône | |
France | CHU de Reims, Néphrologie | Reims | |
France | Centre d'Investigation Clinique CHU de Nancy | Vandoeuvre-les-Nancy |
Lead Sponsor | Collaborator |
---|---|
Centre Hospitalier Universitaire de Besancon | Agence de La Biomédecine, Central Hospital, Nancy, France, Centre Hospitalier Universitaire de Strasbourg, Observatoire Régional de la Santé d'Alsace |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Factors associated with renal replacement therapy | Analysis of the association between renal replacement therapy incidence disparities and socioeconomic environment, geographic accessibility to primary and secondary care and medical practice patterns. | Study period: 2010-2014 | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05990660 -
Renal Assist Device (RAD) for Patients With Renal Insufficiency Undergoing Cardiac Surgery
|
N/A | |
Recruiting |
NCT04096547 -
Rivaroxaban in Elderly NVAF Patients With or Without Renal Impairment
|
||
Completed |
NCT04024332 -
Study of the Way the Body Takes up, Distributes, and Gets Rid of ACT-541468 in Subjects With Abnormal Kidney Function Compared to Healthy Subjects
|
Phase 1 | |
Active, not recruiting |
NCT03672110 -
Slow and Low Start of a Tacrolimus Once Daily Immunosuppressive Regimen
|
Phase 3 | |
Completed |
NCT01407874 -
A Randomized, Double-Blind, Dose-Response Study of the Safety and Uric Acid Effects of Oral Ulodesine Added to Allopurinol in Subjects With Gout and Concomitant Moderate Renal Insufficiency
|
Phase 2 | |
Completed |
NCT01462136 -
PK Study of ACHN-490 Injection in Renally Impaired Subjects
|
Phase 1 | |
Completed |
NCT01172431 -
Indapamide Versus Hydrochlorothiazide in Elderly Hypertensive Patients With Renal Insufficiency
|
Phase 4 | |
Completed |
NCT01545531 -
Two-Point Measurement of Glomerular Filtration Rate by Iohexol Plasma Disappearance
|
N/A | |
Completed |
NCT00770081 -
Safety and Tolerability of Vildagliptin Versus Sitagliptin in Patients With Type 2 Diabetes and Severe Renal Insufficiency (28-week Extension Study)
|
Phase 3 | |
Completed |
NCT00765830 -
Safety and Tolerability of Vildagliptin Versus Placebo in Patients With Type 2 Diabetes and Moderate or Severe Renal Insufficiency (28 Week Extension)
|
Phase 3 | |
Terminated |
NCT00338455 -
Natrecor (Nesiritide) in Transplant-Eligible Management of Congestive Heart Failure-TMAC
|
Phase 2 | |
Completed |
NCT00159614 -
Effect of KW-3902IV in Combination With IV Furosemide on Renal Function in Subjects With CHF and Renal Impairment
|
Phase 2 | |
Completed |
NCT02894905 -
A Study to Evaluate the Effect of Renal Impairment on the Pharmacokinetics of AL-335
|
Phase 1 | |
Completed |
NCT02894385 -
Effect of Hepatic and Renal Impairment on the Pharmacokinetics, Safety and Tolerability of BAY1841788 (ODM-201)
|
Phase 1 | |
Active, not recruiting |
NCT04876963 -
HOLT-ED: Holter-monitoring in End-stage Renal Disease
|
||
Not yet recruiting |
NCT03899298 -
Safety and Clinical Outcomes With Amniotic and Umbilical Cord Tissue Therapy for Numerous Medical Conditions
|
Phase 1 | |
Completed |
NCT03235375 -
A Study to Evaluate Pharmacokinetics, Safety and Tolerability of MEDI0382 in Renal Impairment Subjects
|
Phase 1 | |
Withdrawn |
NCT03329612 -
Remote Ischemic Preconditioning in ACS Patients
|
N/A | |
Recruiting |
NCT02578784 -
DEB-after-Cutting Balloon-PTA in Dialysis Fistula Stenosis
|
N/A | |
Active, not recruiting |
NCT02598635 -
Effects of Cholecalciferol on Osteoprotegerin Levels in Patients on Peritoneal Dialysis
|
Phase 4 |