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Clinical Trials in France / NCT02900040
Recruiting Observational

Clinical Database Associated With a Biological Banking Accessible to Initiate Epidemiological and Translational Collaborative Researches in Kidney Transplantation

NCT02900040 · tracked via the Priya Life Science France tracker
Sponsor
Nantes University Hospital
Phase
Observational
Started
1994-01
Last updated
2016-09-15

Condition(s) studied

Kidney Transplantation

Investigational drug(s) / intervention(s)

kidney transplantation

Study summary

The French DIVAT (standing for Données Informatisées et VAlidées en Transplantation in french, and in English "Computerized and VAlidated Data in Transplantation" ) cohort was Kicked off in 1994 by the Transplantation Urology Nephrology Institute of the Nantes University Hospital in France. The primary objective of this multicenter computerized database was to enable prospective clinical and epidemiological research studies concerning kidney transplant recipients, particularly focusing on mid- and long-term clinical outcomes, therapeutic strategies and public health issues. The patient-case system of the DIVAT cohort allows the monitoring of medical records of all patient-specific and allograft-specific data, including bio-banking since 2005. Data are collected from the date of transplantation until the graft failure, at each scheduled outpatient visit or hospital admission motivating by a new clinical, therapeutical or biological expression. The DIVAT cohort contains information on more than 11000 transplant recipients between 1994 and today, issued from 8 French university hospitals centers (the DIVAT Network is organized by a consortium agreement). 18% of all patients underwent retransplantation and 11% of all kidney transplants originated from living donors. The DIVAT network heavily works to ensure a high-quality data collection with the aim of exploring adequately the complex post-transplantation process. The Divat network encourage collaborations and enables interested researchers to submit a research project by completing a request form available on the DIVAT website (http://www.divat.fr/en) describing the context, objectives and design of the study

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * over the age of 18 years * with renal transplant Exclusion Criteria: * minor * pediatric transplantation

Primary outcome measure(s)

  • Proportion of participants with Overall Survival — 2 years
  • Proportion of participants with Overall Survival — 4 years
  • Proportion of participants with Overall Survival — 6 years

Trial sites (8)

FacilityCityRegionStatus
Docteur Buron Lyon France Recruiting
Professeur Mourad Montpellier France Recruiting
Professeur Kessler Nancy France Recruiting
Professeur Ladriere Nancy France Recruiting
Pr Cassuto Nice France Recruiting
Professeur Kreis Paris France Recruiting
Professeur Legendre Paris France Recruiting
Professeur Rostaing Toulouse France Recruiting

More Nantes University Hospital trials in France

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Evolution of Different Sensitivity Levels in Patients With Chronic Neuropathic Pain in the Pelvi-perineal Region After Treatment With High-concentration Capsaicin Patches Starting soon
Frequency and Intensity of Inflammatory Relapses in Patients With Non-infectious Posterior Uveitis Treated With a Fluocinolone Acetonide Implant Starting soon
Characterization and Support for Neurodevelopmental Disorders Associated With Congenital Heart Defects Recruiting

Other trials for the same condition

CMV-associated Immunomodulation in Renal Transplant Patients Starting soon
Quantiferon CMV to Identify Treatment Need for Asymptomatic CMV Infection After Solid Organ Transplant (QUANTIFOT) Recruiting
Impact of ExtraCorporeal Phototherapy (ECP) on Auxiliary Follicular T-lymphocytes and Circulating B-lymphocytes During Chronic AntiBody-Mediated Rejection in Kidney Transplantation. Recruiting
Salivary Replication of BK Virus in Post-kidney Transplant Starting soon
TTV-based mAnagement Of Long-term ImmunosuppreSsion in Kidney Transplantation Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT02900040 on ClinicalTrials.gov ↗ ← All trials in France