Efficacy of Cyclosporine Ophthalmic Emulsion in the Treatment of Dry Eye Syndrome in Contact Lens Wearers

NCT ID: NCT00335114

Last Updated: 2023-05-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2005-11-30

Study Completion Date

2006-04-30

Brief Summary

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Cyclosporine Ophthalmic Emulsion is currently used in the treatment of dry eye syndrome. Contact lens wearers frequently suffer from dry eye syndrome. The purpose of this study is to evaluate cyclosporine ophthalmic emulsion verses re-wetting drops in the relief of dry eye symptoms in contact lens wearers

Detailed Description

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Conditions

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Contact Lens Wearers With Dry Eye Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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cyclosporine ophthalmic emulsion

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* contact lens wearer
* clinical diagnosis of dry eye syndrome

Exclusion Criteria

\-
Minimum Eligible Age

19 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Alabama at Birmingham

OTHER

Sponsor Role lead

Responsible Party

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Carol E. Rosenstiel

Professor, Director of Contact Lens Service

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Carol E Rosenstiel, OD

Role: PRINCIPAL_INVESTIGATOR

University of Alabama at Birmingham

Locations

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UAB Ophthalmology Services Foundation

Birmingham, Alabama, United States

Site Status

Countries

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United States

Other Identifiers

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F051025017

Identifier Type: -

Identifier Source: org_study_id

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