Expired Study
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San Diego, California 92103


Purpose:

The objective of the study was to evaluate whether timolol hemihydrate is more comfortable upon instillation than timolol maleate in sorbate. This was an observational study. Subjects with open-angle glaucoma or ocular hypertension were asked to complete a survey regarding their normal treatment. No treatment was prescribed.


Criteria:

Inclusion Criteria: - willing to comply with investigator's and protocol's instructions - patients signature on the informed consent document - open-angle glaucoma or ocular hypertension - currently prescribed timolol hemihydrate (once a day (QD) or twice a day (BID))or timolol maleate in sorbate QD as monotherapy or as a part of 2-drug therapy in at least one eye Exclusion Criteria: - inability to understand the trial procedures - inability to give informed consent - inability to understand, read, or write English - best corrected visual acuity of 20/200 or worse in each eye - current moderate to severe infectious or inflammatory condition of the eye or eyelids including - current moderate to severe dry eye syndrome - current chronic use of ocular corticosteroids, ocular surgery or intraocular laser surgery to either eye in the prior 3 months - treated with 3 or more glaucoma medicines in both eye


NCT ID:

NCT00823043


Primary Contact:

Study Director
William C. Stewart, MD
PRN Pharmacuetical Research Network, LLC


Backup Contact:

N/A


Location Contact:

San Diego, California 92103
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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