Phase 4 Study Comparing IOP Lowering in OAG or OH in Caucasian or Japanese Subjects C-02-32

Phase 4

Terminated

• Conditions: Open-angle Glaucoma; Ocular Hypertension

• Registration Number: NCT00047606
• Lead Sponsor: Alcon Research

Brief Summary

The purpose of this study is to evaluate safety and efficacy of two different IOP lowering medications after six weeks of treatment in Caucasian and Japanese subjects.

Detailed Description

Not available

Study Timeline

• Study Start: 2002-08
• Study First Submitted: 2002-10-08
• Study First Submitted QC: 2002-10-10
• Study First Posted: 2002-10-11
• Primary Completion: 2003-11
• Study Completion: 2003-11
• Status Verified: 2008-08
• Last Update Submitted: 2012-08-16
• Last Update Posted: 2012-08-17

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 84

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL