Orientation of the Lymphocyte Response to the Occurrence of Atherosclerotic Complications After Kidney Transplantation
NCT ID: NCT02843867
Last Updated: 2022-08-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
1150 participants
OBSERVATIONAL
2008-11-28
2030-10-23
Brief Summary
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The investigators therefore propose to study the impact of the expansion of regulatory T cells on the risk of atherosclerotic complications after transplantation.
Since November 2008, the investigators began a multicenter, prospective study whose purpose is to study in detail the immunological mechanisms of atherosclerosis after transplantation via immunomonitoring cohort of renal transplant patients in the Grand East Interregion. It was planned to include 500 patients and to date a little more than half have been included. After completion of the blood test, the tubes are routed over the Biomonitoring Platform (CIC-BT 506 Besançon) and the samples are stored in CRB Dijon.
The atherosclerotic events are recorded prospectively. The investigators hope to implement as part of ORLY IS, a second study to determine the impact of an expansion of regulatory T cells on the risk of atherosclerotic events.
Our hypothesis is that a cell rate regulatory T below the median results in an increase of 5% of atherosclerotic complications.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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blood sample
36 ml of blood sample at D0 and 1 year after transplantation
Eligibility Criteria
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Inclusion Criteria
2. Patients receiving a renal transplant
3. Patients able to understand the benefits and risks of testing
4. Patients gave written informed consent.
Exclusion Criteria
2. Immunosuppressive therapy immediately prior to transplantation
3. Cancer (except skin cancer) or malignant blood disease being treated; active infection; decompensated cirrhosis \[patients had cancer and considered as cured or in remission, patients with virus infection of hepatitis B or hepatitis C and having no cirrhosis may be included\].
This study is strictly non-interventional, participation in another study is not a cons-indication to the inclusion in this study and no exclusion period is required for inclusion in another study after inclusion in this study (Art L. 1121-12 (loi n°2004-806 du 9 Août 2004).
18 Years
ALL
No
Sponsors
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University of Franche-Comté
OTHER
Etablissement Français du Sang
OTHER
Centre Hospitalier Universitaire de Besancon
OTHER
Responsible Party
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Principal Investigators
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Didier Ducloux, Pr.
Role: PRINCIPAL_INVESTIGATOR
CHRU de Besançon
Locations
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CHU de Besançon
Besançon, , France
CHU Clermont-Ferrand, 58 rue Montalembert, 63003 Clermont-Ferrand
Clermont-Ferrand, , France
CHU Dijon, Hôpital du Bocage, 2 Bd du Maréchal de Lattre de Tassigny, 21079 Dijon cedex
Dijon, , France
Hôpital du Kremlin Bicêtre 78, rue du Général Leclerc, 94275 Le Kremlin-Bicêtre Cedex
Le Kremlin-Bicêtre, , France
CHU Brabois, et Vandoeuvre les Nancy
Nancy, , France
CHU Reims, 45 rue Cognacq-Jay 51092 Reims Cedex
Reims, , France
Hôpital Civil- 1, place de l'hôpital BP426 ; 67091 Strasbourg Cedex
Strasbourg, , France
Countries
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References
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Ducloux D, Courivaud C, Bamoulid J, Crepin T, Gaiffe E, Laheurte C, Vauchy C, Rebibou JM, Saas P, Borot S. Immune phenotype predicts new onset diabetes after kidney transplantation. Hum Immunol. 2019 Nov;80(11):937-942. doi: 10.1016/j.humimm.2019.08.006. Epub 2019 Sep 10.
Ducloux D, Legendre M, Bamoulid J, Rebibou JM, Saas P, Courivaud C, Crepin T. ESRD-associated immune phenotype depends on dialysis modality and iron status: clinical implications. Immun Ageing. 2018 Jul 17;15:16. doi: 10.1186/s12979-018-0121-z. eCollection 2018.
Other Identifiers
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R/2011/44
Identifier Type: -
Identifier Source: org_study_id
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