Clinical Trials Directory

Trials / Completed

CompletedNCT00379834

12-Month Stability of Diurnal IOP Control on Cosopt

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

Summary

To determine the stability of diurnal intraocular pressure in eyes with glaucoma treated with Cosopt

Detailed description

Glaucoma is a potentially-blinding but treatable eye disease. A major risk factor for glaucoma is elevated intraocular pressure (IOP). IOP is a dynamic variable (like blood pressure)-it changes over time. The more it changes, the more likely patients are to get worse. Glaucoma is treated by lowering IOP. Cosopt is a medication that lowers IOP. Little is known about how well Cosopt reduces IOP fluctuations. In this study, we plan to measure the IOP in both eyes of 10 glaucoma patients treated with Cosopt, every 2 hours from 8am to 8pm, on five separate days over a one-year period. Untreated baseline IOP will be measured on a similar long day before beginning treatment with Cosopt. This methodology will allow us to compare IOP fluctuations with and without Cosopt, and also to learn about long-term control of IOP fluctuations in eyes treated with Cosopt.

Conditions

Interventions

TypeNameDescription
DRUGCosoptCosopt twice daily in both eyes

Timeline

Start date
2006-09-01
Primary completion
2008-04-01
Completion
2008-04-01
First posted
2006-09-25
Last updated
2015-02-10
Results posted
2015-02-10

Source: ClinicalTrials.gov record NCT00379834. Inclusion in this directory is not an endorsement.