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

N/ACompletedNCT01139372

Alcon Research96 enrolled

Overview

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

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Dry Eye

Interventions

FID 115958D (Lubricant Eye Drop)OTHER

1 drop in each eye at least twice daily

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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

Outcomes

Primary Outcomes

Daytime Use Assessment: "I would use this product at bedtime for my dry eye symptoms" Likert scale (i.e. strongly disagree, disagree, neither disagree nor agree, agree, strongly agree)

Time frame: Day 7

Data from ClinicalTrials.gov

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