Acute Comfort of Lubricant Eye Drop FID 111421

To evaluate the acute comfort and blurring profile between two artificial tears products in dry eye patients

Completed

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Key information

Conditions

Dry Eye Dry Eye Syndromes Eye Diseases Lacrimal Apparatus Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Documented diagnosis of dry eye
Must not have worn contact lenses for 1 week preceding enrollment

Exclusion criteria

Age related

Treatment and study plan

Lubricant Eye Drop FID 111421

Other

Lubricant Eye Drop FID 111421 1 drop each eye one time

Optive Lubricant Eye Drop

Other

Optive Lubricant Eye Drop 1 drop each eye one time

Primary outcomes

Drop Comfort Upon Instillation

Time frame: upon instillation

Drop comfort grading scale is a scale from 0 to 9, with 0 meaning most comfortable and 9 meaning most uncomfortable.

Sponsors and collaborators

Lead sponsor

Alcon Research

Industry

Registry information

Important dates

Study start: 2007
Primary completion: 2008
First posted: May 7, 2008
Registry last updated: Feb 2, 2012

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.

Published trials that share one or more normalized conditions with this study.

Completed