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OpenTrials
Completed

NCT Number: NCT01076998

Acute Comfort and Blur Profile of a Lubricant Eye Drop Versus a Marketed Eye Ointment

The purpose of this study is to compare the comfort and blurriness of the investigational lubricant eye drop with a marketed artificial tear ointment.

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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

Exclusion criteria

  • Must not have worn contact lenses within 12 hours preceding enrollment
  • Must not have used any topical ocular drops or ointment within 24 hours preceding enrollment

Treatment and study plan

Lubricant eye drop FID 115958D

Other

1 drop in each eye, one time

Refresh PM Ointment

Other

1 drop in each eye, one time

Primary outcomes

  1. Three-minute visual blur profile

    Time frame: Through 3 minutes (post-instillation)

  2. Overall Acceptability

    Time frame: Immediately upon instillation

Secondary outcomes

  1. Drop Comfort Upon Instillation

    Time frame: Immediately upon installation

Sponsors and collaborators

Lead sponsor

Alcon Research

Industry

Registry information

Important dates

Study start
2010
Primary completion
2010
First posted
Feb 26, 2010
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.

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