Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | cyclosporine and sodium carboximethycellulose | Ten 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 |
| DRUG | sodium carboximethycellulose | Ten 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.