An Evaluation of the Daytime Use of an Investigational Lubricant Eye Drop

NCT ID: NCT01139372

Last Updated: 2012-02-02

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 96 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-05-31
• Study Completion Date: 2010-06-30

Brief Summary

The purpose of this study is to describe the subjective assessments of an investigational lubricant eye drop.

Conditions

Dry Eye

Study Design

• Allocation Method: NON_RANDOMIZED
• 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 least twice daily

Interventions

FID 115958D (Lubricant Eye Drop)

1 drop in each eye at least twice daily

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Documented diagnosis of dry eye
• Current use of Refresh Liquigel, GenTeal Gel Drops or Refresh Celluvisc at least twice daily

Exclusion Criteria

• Must not have worn contact lenses within 7 days preceding enrollment
• 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-10-006

Identifier Type: -

Identifier Source: org_study_id