Patient Preference Comparison of AZARGA Versus COSOPT

Status Completed

Clinical Trial Summary

The purpose of this study was to assess patient preference regarding ocular comfort of AZARGA® compared to COSOPT® after one week instillation of each study medication.

Clinical Trial Description

At the Screening Visit, each intervention was instilled in one eye in a contralateral fashion to establish baseline ocular comfort prior to randomization. A 48-hour washout period separated the two treatment periods. ;

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01340014
Study type	Interventional
Source	Alcon Research
Contact
Status	Completed
Phase	Phase 4
Start date	September 2011
Completion date	October 2012

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