Clinical Trials Directory

Trials / Terminated

TerminatedNCT00463723

Topical FK506 (Tacrolimus) for Prevention of Immune Reactions Following Penetrating Keratoplasty

Status
Terminated
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
Sponsor
University Hospital Freiburg · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Background: Patients following allogeneic keratoplasty are treated with topical and frequently with systemic steroids to prevent immune reactions. Steroids are known to yield good results, but exert a wide range of side effects. The efficacy of topial FK506 in preventing immune reactions has already been demonstrated experimentally. FK506, an IL-2-inhibitor like Cyclosporin A (CSA), is known to be approximately 100 fold more potent than CSA. Aim of the study: In this study the efficacy and safety of topical FK506 will be compared to our standard treatment (i.e. steroids) after penetrating normal-risk keratoplasty.

Conditions

Interventions

TypeNameDescription
DRUGFK506 0.06% (eye drops)

Timeline

First posted
2007-04-20
Last updated
2007-04-20

Source: ClinicalTrials.gov record NCT00463723. Inclusion in this directory is not an endorsement.

Topical FK506 (Tacrolimus) for Prevention of Immune Reactions Following Penetrating Keratoplasty (NCT00463723) · Clinical Trials Directory