At a glance
ClinicalIndex Comparison RecordPhase 4Completed· 10 enrolled
Drug / intervention
Cosoptdrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
12-Month Stability of Diurnal IOP Control on Cosopt
In Brief
A Phase 4 clinical trial evaluating Cosopt for Glaucoma. Completed, enrolled 10 participants.
Detailed Summary
To determine the stability of diurnal intraocular pressure in eyes with glaucoma treated with Cosopt
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsGlaucoma
Countries--
Collaborators--
Timeline
Phase 4CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartSep 2006
First PostedSep 2006
Primary CompletionApr 2008
TodayJul 2026
First PostedSep 25, 2006
Enrollment StartSep 1, 2006
Primary CompletionApr 1, 2008
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 19.8 years ago
Interventions
Cosoptdrug
Cosopt twice daily in both eyes