A Multi-Center Randomized Study to Evaluate the Efficacy and Safety of an Investigational Lubricant Eye Drop

Phase 2

Completed

• Conditions: Dry Eye

• Registration Number: NCT00243711
• Lead Sponsor: Allergan

Brief Summary

The efficacy, safety and acceptability of an investigational lubricant eye drop in subjects with dry eye will be evaluated in comparison with currently-available lubricant eye drops.

Detailed Description

Not available

Study Timeline

• Study Start: 2005-09
• Study First Submitted: 2005-10-21
• Study First Submitted QC: 2005-10-21
• Study First Posted: 2005-10-25
• Primary Completion: 2006-04
• Study Completion: 2006-04
• Status Verified: 2011-05
• Last Update Submitted: 2011-05-27
• Last Update Posted: 2011-05-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 286

Inclusion Criteria

• Mild, Moderate, or Severe Dry Eye Symptoms and current eye drop use;
• Reduced tear stability or tear production

Exclusion Criteria

• NONE

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Dry Eye Symptoms

Secondary Outcome Measures

Name	Time	Method
Ocular surface damage, tear stability, tear production