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A Prospective Randomized Trial on Mycophenolate Mofetil in Risk Penetrating Keratoplasty

Corneal Transplantation Clinical Trial

Clinical Trial Summary

The purpose of this prospectively randomized multicentre study was to prove the efficacy and safety of mycophenolate mofetil (MMF) to preventing graft rejection and improvement of clear graft survival following high-risk keratoplasty.

The patients of the MMF group receive MMF orally 2x1 g daily for 6 months. Endpoints were immune reaction free and clear graft survival and the occurence of side-effects.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00411515
Study type Interventional
Source University Hospital Freiburg
Contact
Status Completed
Phase Phase 4
View Details
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