Acute Comfort of Lubricant Eye Drop FID 111421

NCT ID: NCT00673959

Last Updated: 2012-02-02

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-12-31

Brief Summary

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To evaluate the acute comfort and blurring profile between two artificial tears products in dry eye patients

Detailed Description

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Conditions

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Dry Eye

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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Lubricant Eye Drop FID 111421

Lubricant Eye Drop FID 111421 1 drop each eye one time

Group Type EXPERIMENTAL

Lubricant Eye Drop FID 111421

Intervention Type OTHER

Lubricant Eye Drop FID 111421 1 drop each eye one time

Optive Lubricant Eye Drop

Optive Lubricant Eye Drop 1 drop each eye one time

Group Type ACTIVE_COMPARATOR

Optive Lubricant Eye Drop

Intervention Type OTHER

Optive Lubricant Eye Drop 1 drop each eye one time

Interventions

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Lubricant Eye Drop FID 111421

Lubricant Eye Drop FID 111421 1 drop each eye one time

Intervention Type OTHER

Optive Lubricant Eye Drop

Optive Lubricant Eye Drop 1 drop each eye one time

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Documented diagnosis of dry eye
* Must not have worn contact lenses for 1 week preceding enrollment

Exclusion Criteria

* Age related
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Alcon Research

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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C-07-08

Identifier Type: -

Identifier Source: org_study_id

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