Cross-Over Evaluation of Two Lubricating Eye Drops

To evaluate the efficacy of two lubricating eye drops for the treatment of dry eye signs and symptoms.

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

Phase 4

Primary location

Hazleton Eye Specialists

Hazleton, Pennsylvania, 18202, United States

Who can participate

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

Inclusion criteria

Patients 18 yrs or older
Males or females
Any race or ethnic background
Patients with present ocular surface discomfort and a SESoD score of at least 2

Exclusion criteria

Corneal refractive surgery within 6 months of this study.
Contact lens use on day of examination.
Corneal ectasia.
Current use of Restasis

Treatment and study plan

Polyethylene Glycol 400 0.4%

Drug

Propylene Glycol 0.3%

Drug

0.15% sodium Hyaluronate

Drug

Sodium Chloride

Drug

sodium phosphate monobasic

Drug

Sponsors and collaborators

Lead sponsor

Innovative Medical

Industry

Registry information

Important dates

First posted: Jun 28, 2007
Registry last updated: Jan 15, 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.

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

Completed