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OpenTrials
Completed

NCT Number: NCT00473070

A Clinical Study of Tobradex AF

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.

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Key information

Conditions

Cataract Eye Diseases Lens Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Pittsburgh

Pittsburgh, Pennsylvania, 15122, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients requiring cataract surgery

Exclusion criteria

  • Age related

Treatment and study plan

Tobradex AF

Drug

Primary outcomes

  1. Concentration of dexamethasone in aqueous humor following a single topical ocular administration

    Time frame: Periodic

Secondary outcomes

  1. Changes in external and internal ocular structures, intraocular pressure, vision and other side effects

    Time frame: Periodic

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Completed

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Sponsors and collaborators

Lead sponsor

Alcon Research

Industry

Registry information

Important dates

Study start
2006
Primary completion
2007
First posted
May 14, 2007
Registry last updated
Jul 29, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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