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Dry Eye Symptom Relief Assessment With Use of TrueTear in a Controlled Adverse Environment

Dry Eye Clinical Trial

Official title:
Prospective, Single-Arm Clinical Trial to Evaluate Acute Dry Eye Symptom Relief Assessed During Exposure to a Controlled Adverse Environment (CAE®) Following a 45 Day Period With Application of TrueTear™

Clinical Trial Summary

This study characterizes acute dry eye symptom control, assessed during exposure to a Controlled Adverse Environment, following use of the TrueTear for 45 days.

Clinical Trial Description

Subjects will be instructed to use the TrueTear daily for approximately 45 days with assessments in the Controlled Adverse Environment taking place on Day 0 and Day 45. Upon entering the CAE, participants will complete dry eye symptom questionnaires every five minutes and will administer the device when a certain level of ocular discomfort has been reached. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03097614
Study type Interventional
Source Oculeve, Inc.
Contact
Status Completed
Phase N/A
Start date March 31, 2017
Completion date June 26, 2017
View Details
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