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OpenTrials
Completed

NCT Number: NCT00347854

Fluorophotometry Evaluation of Lubricant Eye Drops

The objective of this study is to evaluate the safety and efficacy of exaggerated use of Lubricant Eye Drops in a population of normal subjects by measuring corneal epithelial permeability to fluorescein.

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Key information

Conditions

Healthy

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Alcon

Fort Worth, Texas, 76134, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Ages 18 and over

Exclusion criteria

  • No sodium fluorescein corneal staining at Screening Visit

Treatment and study plan

Systane Free Lubricant Eye Drops

Other

Visine Tears Lubricant Eye Drops

Other

Refresh Liquigel Lubricant Eye Drops

Other

Refresh Plus Lubricant Eye Drops

Other

Primary outcomes

  1. Epithelial permeability to fluorescein

Secondary outcomes

  1. tear turnover rate

Sponsors and collaborators

Lead sponsor

Alcon Research

Industry

Registry information

Official study title

Fluorophotometry Evaluation of Lubricant Eye Drops FID 105783

Important dates

Study start
2006
Primary completion
2006
Study completion
2006
First posted
Jul 4, 2006
Registry last updated
Nov 22, 2016

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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