Study of the Effects of Artificial Tears on the Response to the Latanoprost Punctal Plug Delivery System in Subjects With Ocular Hypertension or Open-Angle Glaucoma
Completed · Phase 2
Conditions studied: Glaucoma, Ocular Hypertension
In brief
The purpose of this study is to determine the effect of artificial tears preserved with Benzalkonium Chloride (AT-BAK) on the IOP response to the L-PPDS and to evaluate the safety of the L-PPDS in subjects with OH or OAG following treatment.
Key facts
- Study ID
- NCT00845299
- Run by
- Mati Therapeutics Inc.
- People needed
- 40
- Starts
- 2009-01-01
- Expected to finish
- 2009-12-01
- Last updated by the study team
- 2013-09-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Over 18 years with ocular hypertension or open-angle glaucoma
- Subjects who have a best-corrected visual acuity of 20/100 or better
You may not qualify if…
- Subjects who wear contact lenses
- Uncontrolled medical conditions
- Subjects with a known sensitivity to latanoprost, BAK, or any other products required for the study
- Subjects requiring chronic topical artificial tears, lubricants, and/or requiring any other chronic topical medications.
Where it is running
- Study site — Menlo Park, California, United States
Full record on ClinicalTrials.gov
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