Soothe Versus Refresh

To determine the ocular efficacy and safety of Soothe and Refresh Tears.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

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

Coastal Research Associates, LLC, Atlanta, Georgia, United States

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

adults with a diagnosis of dry eyes
Schirmer's with anesthesia grade between 1-7 mm inclusive after five (5) minutes in at least one eye
a corneal staining grade of greater than or equal to 2 (scale 0-4) in the same qualifying eye as the Schirmer's test

Exclusion criteria

contact lens use during the active treatment periods of the trial
history of Sjogren's Syndrome
temporary punctal occlusion that is still effective
the current or anticipated use during the study of punctual plugs
current treatment with Restasis

Treatment and study plan

Soothe

Drug

Refresh Tears

Drug

Sponsors and collaborators

Lead sponsor

Pharmaceutical Research Network

Other

Registry information

Important dates

Study completion: 2006
First posted: Feb 1, 2006
Registry last updated: Aug 22, 2006

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