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
| Type | Name | Description |
|---|---|---|
| OTHER | no intervention, this is an observational retrospective trial | no 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.