Clinical Trials Directory

Trials / Completed

CompletedNCT01488396

Efficacy of 0.05% Cyclosporin Eye Drop in Stevens Johnson Syndrome Patient With Chronic Dry Eye

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
31 (actual)
Sponsor
Mahidol University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the efficacy of 0.05% cyclosporin ophthalmic emulsion (Restasis) in patients with Stevens-Johnson syndrome that have dry eyes by subjective symptoms and signs.

Detailed description

Stevens-Johnson syndrome patients in chronic stage who have dry eys symptoms and signs will be treated with 0.05%cyclosporin ophthalmic emulsion(Restasis)twice a day for 6 months, compare results at 0,2,4,6 months include dry eye symptoms, corneal staining (Fluorescein, Rose Bengal), Schirmer I,FCT and impression cytology

Conditions

Interventions

TypeNameDescription
DRUG0.05%cyclosporin eye dropuse twice daily for 6 months

Timeline

Start date
2007-02-01
Primary completion
2009-07-01
Completion
2009-07-01
First posted
2011-12-08
Last updated
2011-12-08

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT01488396. Inclusion in this directory is not an endorsement.