Acute Comfort and Blur of Systane and Optive

NCT ID: NCT00568386

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

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-11-30

Study Completion Date

2007-12-31

Brief Summary

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To evaluate drop comfort, acceptability, preference and blur profile between two marketed artificial tears in both dry eye and non-dry eye patient population.

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

DOUBLE

Study Groups

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Systane Lubricant Eye Drops

Systane Lubricant Eye Drops 1 drop in each eye one time

Group Type EXPERIMENTAL

Systane Lubricant Eye Drops

Intervention Type OTHER

Systane Lubricant Eye Drops 1 drop each eye once time

Optive Lubricant Eye Drops

Optive Lubricant Eye Drops 1 drop each one time

Group Type ACTIVE_COMPARATOR

Optive Lubricant Eye Drops

Intervention Type OTHER

Optive Lubricant Eye Drops 1 drop each eye one time

Interventions

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Systane Lubricant Eye Drops

Systane Lubricant Eye Drops 1 drop each eye once time

Intervention Type OTHER

Optive Lubricant Eye Drops

Optive Lubricant Eye Drops 1 drop each eye one time

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Healthy, normal eyes OR documented diagnosis of dry eye

Exclusion Criteria

* Must not have worn contact lenses for 7 days preceding enrollment
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Alcon Research

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Mike Christensen

Role: PRINCIPAL_INVESTIGATOR

Alcon Research

Other Identifiers

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M-07-02

Identifier Type: -

Identifier Source: org_study_id

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