Clinical Trials Directory

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UnknownNCT00797030

Topical Cyclosporine for the Treatment of Dry Eye in Patients Infected With the Human Immunodeficiency Virus

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Universidade Federal do Rio de Janeiro · Academic / Other
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

This study evaluates the use of topical cyclosporine 0.05% and sodium carboxymethylcellulose 0.5% for the treatment of dry eye disease in patients infected with the human immunodeficiency virus. Twenty HIV-positive-patients were selected from the Department of Infectious Diseases of the Federal University of Rio de Janeiro Hospital. Dry eye diagnosis was based on a dry eye questionnaire (Ocular Surface Disease Index - OSDI®), Schirmer I Test, break up time and 1% rose bengal staining of the ocular surface. The patients were divided into two groups with ten patients. Group I received sodium carboxymethylcellulose 0.5% drops and group II received sodium carboxymethylcellulose 0,5% drops and topical cyclosporine 0.05% for six months.

Conditions

Interventions

TypeNameDescription
DRUGcyclosporine and sodium carboximethycelluloseTen HIV-positive patients with dry eye received sodium carboximethylcellulose 0.5% (one drop 4 times per day) and topical cyclosporine 0.05% (one drop twice a day) during six months
DRUGsodium carboximethycelluloseTen HIV-positive patients with dry eye received sodium carboximethycellulose (1 drop 4 times per day) during six months

Timeline

Start date
2006-10-01
Primary completion
2008-07-01
Completion
2008-11-01
First posted
2008-11-24
Last updated
2008-11-24

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT00797030. Inclusion in this directory is not an endorsement.