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

Alcon

Status: Completed

Conditions: Dry Eye

Treatments: Other: FID 115958D (Lubricant Eye Drop)

Study type: Interventional

Funder types: Industry

Identifiers

NCT01139372

C-10-006

Details and patient eligibility

About

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

Enrollment: 96 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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96 participants in 1 patient group

FID 115958D

Experimental group

Description:

Lubricant eye drop

Treatment:

Other: FID 115958D (Lubricant Eye Drop)