Clinical Trials Directory

Trials / Completed

CompletedNCT00705510

Efficacy of 0.05 % Cyclosporine Ophthalmic Emulsion Compare With Tear in Meibomian Gland Dysfunction

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

Summary

To evaluate the efficacy of 0.05% cyclosporine ophthalmic emulsion (Restasis® , Allergan) versus an artificial tears alone in patients with meibomian gland dysfunction that have abnormal tear quality and quantity by subjective symptoms and signs including tear breakup time

Detailed description

Meibomian gland dysfunction patients will divide into 2 groups. One group will have 0.05% cyclosporine opthalmic emulsion and the other will have non-preservative artificial tear twice daily, compare the result in 3 months.

Conditions

Interventions

TypeNameDescription
DRUG0.05% cyclosporin eye dropuse the medication twice daily for 3 months

Timeline

Start date
2008-05-01
Primary completion
2010-10-01
Completion
2010-10-01
First posted
2008-06-26
Last updated
2010-11-09

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT00705510. Inclusion in this directory is not an endorsement.