Clinical Trials Directory

Trials / Completed

CompletedNCT01496703

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

Reasons for Dose Reduction of Mycophenolate Mofetil During the First Post-transplant Year in Renal Transplant Recipients and Its Impact on Graft Outcome: a Single-center Retrospective Analysis

Status
Completed
Phase
Study type
Observational
Enrollment
749 (actual)
Sponsor
Universitaire Ziekenhuizen KU Leuven · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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 dose reduction which may expose transplant recipients to a higher risk of acute rejection and graft loss. This study's aim was to examine the reasons for MMF dose reduction during the first year after kidney transplantation and its impact on acute rejection, overall and death-censored graft loss. Methods: Retrospective electronic file based analysis of all patients who underwent a single kidney transplantation in our center between 1996 and 2007 and were treated with MMF as part of their initial maintenance immunosuppressive protocol (n=749).

Conditions

Interventions

TypeNameDescription
OTHERno intervention, this is an observational retrospective trialno intervention, this is an observational retrospective trial

Timeline

Start date
1996-01-01
Primary completion
2008-12-01
Completion
2008-12-01
First posted
2011-12-21
Last updated
2011-12-21

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT01496703. Inclusion in this directory is not an endorsement.