Acute Comfort and Blur of Systane Ultra and Systane

NCT ID: NCT00748865

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

2008-07-31

Study Completion Date

2008-08-31

Brief Summary

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To evaluate drop comfort, acceptability, preference and blue profile between two marketed artificial tears in both dry eyes 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

Participants Investigators

Study Groups

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Systane Ultra

Systane Ultra 1 drop each eye one time

Group Type EXPERIMENTAL

Systane Ultra Lubricant Eye Drops

Intervention Type OTHER

Systane Ultra Lubricant Eye Drops 1 drop each eye one time

Systane

Systane 1 drop each eye one time

Group Type ACTIVE_COMPARATOR

Systane Lubricant Eye Drops

Intervention Type OTHER

Systane Lubricant Eye Drops 1 drop each eye one time

Interventions

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Systane Ultra Lubricant Eye Drops

Systane Ultra Lubricant Eye Drops 1 drop each eye one time

Intervention Type OTHER

Systane Lubricant Eye Drops

Systane Lubricant Eye Drops 1 drop each eye one time

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Documented diagnosis of dry eye

Exclusion Criteria

* Use of contact lens within 7 days preceding enrollment
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

Locations

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Contact Alcon Call Center for Trial Location

Fort Worth, Texas, United States

Site Status

Countries

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United States

Other Identifiers

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M-08-09

Identifier Type: -

Identifier Source: org_study_id

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