Expired Study
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La Jolla, California 92093


Purpose:

This study will evaluate the 24-hour IOP-lowering efficacy of 0.01% bimatoprost once daily in patients with glaucoma or ocular hypertension


Criteria:

Inclusion Criteria: - primary open-angle glaucoma or ocular hypertension Exclusion Criteria: - Women of childbearing potential previous glaucoma surgery presence of other eye disease


NCT ID:

NCT01271686


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

La Jolla, California 92093
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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