An Evaluation of the Nighttime Retention of Effect of an Investigational Lubricant Eye Drop (FID 115958D)

NCT ID: NCT01165164

Last Updated: 2012-02-02

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 89 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-06-30
• Study Completion Date: 2010-07-31

Brief Summary

The purpose of this study is to describe the night-time use of an investigational lubricant eye drop.

Conditions

Dry Eye

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

FID 115958D

Lubricant eye drop

Group Type: EXPERIMENTAL

FID 115958D (lubricant eye drop)

Intervention Type: OTHER

1 drop in each eye at bedtime

Interventions

FID 115958D (lubricant eye drop)

1 drop in each eye at bedtime

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. Documented diagnosis of dry eye

2. Current use of an eye ointment or tube gel

Exclusion Criteria

1. No nighttime contact lenses wear throughout the study period

2. Must not have had punctal plugs inserted within 30 days preceding enrollment

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Alcon Research

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

C-10-014

Identifier Type: -

Identifier Source: org_study_id