kidney transplant recipients niertransplantatie patiënten
Conditions
Interventions
None listed
Sponsors
Leiden University Medical Center
Eligibility
Inclusion criteria
Inclusion criteria: Patients who will undergo a kidney retransplant and, if applicable, their living kidney donor
Exclusion criteria
Exclusion criteria: Hepatitis C or HIV seropositive individuals
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main parameter to be assessed in the current study is the frequency of donor-specific memory B cells as determined by a novel ELISPOT based technique. Furthermore, donor-specific antibody levels will be determined by CDC and Luminex techniques. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary study parameters are clinical parameters. The transplant function at 6 and 12 months will be determined by the estimated Glomerular Filtration Rate (eGFR), calculated by the Modification of Diet in Renal Disease (MDRD) formula. Furthermore, the occurrence of cellular and antibody mediated rejection within the first year after transplantation will be recorded. | — |
Contacts
Public ContactS. Heidt
Outcome results
None listed