Phase 3 Study Comparing IOP Lowering in OAG or OH in Japanese Subjects C-01-98

Phase 3

Completed

• Conditions: Ocular Hypertension; Open-Angle Glaucoma

• Registration Number: NCT00047593
• Lead Sponsor: Alcon Research

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2000-01
• Study First Submitted: 2002-10-08
• Study First Submitted QC: 2002-10-10
• Study First Posted: 2002-10-11
• Primary Completion: 2004-07
• Study Completion: 2004-07
• Status Verified: 2008-08
• Last Update Submitted: 2008-08-04
• Last Update Posted: 2008-08-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL