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
| Type | Name | Description |
|---|---|---|
| DRUG | 0.05%cyclosporin eye drop | use 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.