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

N/ACompletedNCT01165164

Alcon Research89 enrolled

Overview

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

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Dry Eye

Interventions

FID 115958D (lubricant eye drop)OTHER

1 drop in each eye at bedtime

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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

Outcomes

Primary Outcomes

Nighttime Use Assessment

Nighttime 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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