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MMF After Pediatric Liver Transplantation

H

Hannover Medical School (MHH)

Status

Completed

Conditions

Chronic Kidney Disease
Liver Transplantation

Treatments

Drug: MMF

Study type

Interventional

Funder types

Other

Identifiers

NCT00367146
MHH3474MMF

Details and patient eligibility

About

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.

Enrollment

25 patients

Sex

All

Ages

Under 17 years old

Volunteers

No Healthy Volunteers

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)

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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