Chronic Kidney Disease Clinical Trial
The use of CNIs (CSA or FK) as primary immunosuppressive drugs after pediatric liver
transplantation is one of the main causes of chronic kidney disease in these patients in the
long term.
The study objective is the evaluation of safety of a modification in immunosuppression from
a dual-immunosuppression (CSA or FK plus steroids) to a triple immunosuppression (MMF plus
CSA (reduced dosage) plus steroids.
Status | Completed |
Enrollment | 25 |
Est. completion date | August 2008 |
Est. primary completion date | August 2008 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A to 17 Years |
Eligibility |
Inclusion Criteria: - patients after pediatric liver transplantation - no acute rejections for the last half year Exclusion Criteria: - concomitant malign disease (e.g. ptld) - neutropenia (granulocytes <1000/µl) - systemic infection - thrombopenia (<80/nl) |
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Germany | Hannover medical School | Hannover |
Lead Sponsor | Collaborator |
---|---|
Hannover Medical School |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | safety of a triple immunosuppression (MMF/CSA/Steroids)regarding the number of acute rejections | 1, 3, 6, 9, 12, 24 month | Yes | |
Secondary | incidence of chronic kidney disease | 12, 24 month | No | |
Secondary | incidence of infections | 1, 3, 6, 9, 12, 24 month | No | |
Secondary | incidence of ptld (post transplant lymphoproliferative disease) | 1, 3, 6, 9, 12, 24 month | No |
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