NCT Number: NCT00273442
Assessing Cosopt Switch Patients
To assess the safety and efficacy of a cohort of patients switched to the dorzolamide/timolol maleate fixed combination because they are insufficiently controlled on latanoprost monotherapy.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Primary location
Little Rock Eye Clinic, Little Rock, Arkansas, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- adults with clinical diagnosis of POAG, pigment-dispersion or exfoliation glaucoma or ocular hypertension
- the IOP on latanoprost must be 31 mm Hg or less in both eyes, and 21 to 31 mm Hg inclusive in at least one eye at 08:00 AM
- visual acuity should be 20/200 or better in each eye
Exclusion criteria
- contraindications to study drugs
- anticipated change in systemic hypotensive therapy during the trial
- use of any corticosteroids by any route in the three months immediately prior to Visit 2
Treatment and study plan
dorzolamide/timolol maleate fixed combination
DrugSponsors and collaborators
Lead sponsor
Pharmaceutical Research Network
Other
Registry information
Important dates
- Study start
- 2005
- Study completion
- 2007
- First posted
- Jan 9, 2006
- Registry last updated
- Nov 19, 2008
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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