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Evaluation of an Early Screening Test of Chronic Rejection and of Operational Tolerance by MicroArray in Renal Graft (Protocol DPRC Array)

Evaluation of an Early Screening Test of Chronic Rejection and of Operational Tolerance by MicroArray in Renal Graft.

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00746057
Enrollment
134
Registered
2008-09-03
Start date
2006-05-31
Completion date
2011-05-31
Last updated
2013-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

First Cadaveric Renal Graft

Keywords

Renal graft, chronic rejection, tolerance, DNA chip, biopsy

Brief summary

The aim of the study is to explore the possibility to identify, at an early stage after a renal graft and from blood samples collected within first months after graft, a predictive transcriptional profile of long term occurence of graft operational tolerance or chronic rejection. The aim of the study is to determine an early transcriptional profile of chronic rejection in the transcriptome of mononuclear blood cells. Validation and predictivity of transcriptional analysis will be based on graft function and graft histology one year after transplantation.The other aim is to determine an early transcriptional profile of operational tolerance in the same patients using a DNA chip dedicated including two lists of genes discriminating tolerant patients who are stopped immunosuppressant treatment for over a year. To allow statistical analysis of 100 patients followed one year after graft, patients not assessable at one year due to early termination of study will be replaced.

Interventions

BIOLOGICALDNA chip

One biopsy is realized before graft, another biopsy is realized one year after graft and a blood sample is collected 3 months after graft to realize DNA chip. Blood samples are also collected at day 0, day 1, month 3, month 6 and month 12 to analyze biochemistry, proteinuria, haematology, creatinine clearance and immunology at day 0, month 3 and month 12.

Sponsors

Nantes University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients aged 18 to 65 years old, * Donor's age ≤ 60 years old, * Patients receiving a first cadaveric renal graft, * Patients taking immunosuppressant treatment including an induction with Simulect at day 0 and day 4, FK 506 (Prograf®) associated with Cellcept and steroids (for three months), * Patients don't taking indispensable anticoagulant treatment.

Exclusion criteria

* Patient's age \< 18 or \> 65 years old, * Donor's age ≥ 60 years old, * Pregnant women or breast feeding women, * Patients receiving a retransplantation, a kidney and pancreas graft or a graft from a living donor, * Patients taking immunosuppressant treatment without FK 506 (Prograf®), Cellcept and steroids. * Patients with coagulation troubles or taking indispensable anticoagulant treatment, * No biopsy before graft.

Design outcomes

Primary

MeasureTime frame
Transcriptional profile (exhaustive DNAchip) on the blood at 3 months post transplantation.3 months

Secondary

MeasureTime frame
Correlation of the transcriptional profile at 3 months after transplantation with histological features of the kidney graft at one year of follow-up.One year

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026