Status:

COMPLETED

Reasons for Mycophenolate Mofetil Dose Reduction and Impact on Graft Outcome in Renal Transplant Recipients

Lead Sponsor:

Universitaire Ziekenhuizen KU Leuven

Conditions:

Acute Rejection of Renal Transplant

Renal Graft Loss

Eligibility:

All Genders

18+ years

Brief Summary

Mycophenolate mofetil (MMF) decreases the risk of acute rejection and is associated with improved graft survival in renal transplant recipients. However, MMF-related side effects often necessitate dos...

Eligibility Criteria

Inclusion

  • All patients who received a single renal transplant at the University Hospitals of Leuven between April 1996 (when MMF was introduced in the Leuven renal transplant program) and February 2007 and were treated with MMF (Cellcept®, Roche) as part of their initial maintenance immunosuppressive regimen were included in this retrospective analysis.

Exclusion

  • If a patient underwent more than one kidney transplantation in the abovementioned 11-year period, only the last was considered.

Key Trial Info

Start Date :

January 1 1996

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

December 1 2008

Estimated Enrollment :

749 Patients enrolled

Trial Details

Trial ID

NCT01496703

Start Date

January 1 1996

End Date

December 1 2008

Last Update

December 21 2011

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Universitaire Ziekenhuizen Leuven

Leuven, Belgium, 3000

Reasons for Mycophenolate Mofetil Dose Reduction and Impact on Graft Outcome in Renal Transplant Recipients | DecenTrialz