A Clinical Study of Tobradex AF

NCT ID: NCT00473070

Last Updated: 2008-07-29

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

PHASE3

Total Enrollment

900 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-11-30

Brief Summary

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The purpose of this study is to determine the amount of study medication that moves from the front of the eye into the fluid at the front of the inside of the eye.

Detailed Description

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Conditions

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Cataract

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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Tobradex AF

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Adult patients requiring cataract surgery

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

Principal Investigators

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Robert Faulkner

Role: STUDY_DIRECTOR

Alcon Research

Locations

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Pittsburgh

Pittsburgh, Pennsylvania, United States

Site Status

Countries

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United States

Other Identifiers

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C-06-37

Identifier Type: -

Identifier Source: org_study_id