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A Study of LUMIGAN® RC in the Clinical Setting

Ocular Hypertension Clinical Trial

Clinical Trial Summary

This study will evaluate bimatoprost 0.01% (LUMIGAN® RC) in patients with elevated intraocular pressure (IOP) due to primary open angle glaucoma (POAG) or ocular hypertension (OHT) in a clinical setting.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01833741
Study type Interventional
Source Allergan
Contact
Status Completed
Phase Phase 4
Start date December 2009
Completion date March 2011
View Details
See also
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