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

Completed · Not applicable

Conditions studied: Dry Eye, Dry Eye Syndromes

In brief

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

Key facts

Study ID

NCT03097614

Run by

Oculeve, Inc.

People needed

57

Starts

2017-03-31

Expected to finish

2017-06-26

Last updated by the study team

2018-10-18

Who can join

Age: 22 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Have used and/or desired to use an artificial tear substitute for dry eye symptoms within 6 months prior to the Screening Visit
• Normal lid/lash anatomy, blinking function and closure as determined by the Investigator
• Literate, able to speak English, and able to complete questionnaires independently

You may not qualify if…

• Chronic or recurrent epistaxis, coagulation disorders or other conditions that, in the opinion of the Investigator, may lead to risk of clinically significant increased bleeding
• Nasal or sinus surgery (including history of application of nasal cautery) or significant trauma to these areas
• Contact lens use within 7 days prior to the Screening Visit or anticipate the use of contact lenses at any time during the study
• Corneal transplant in either or both eyes
• Cardiac demand pacemaker, implanted defibrillator, or other active implanted metallic or active implanted electronic device in the head
• A woman who is pregnant, nursing an infant, or planning a pregnancy during the duration of the study
• Currently enrolled in an investigational drug or device study or have used an investigational drug or device within 30 days prior to the Screening Visit

Where it is running

• Andover Eye Associates — Andover, Massachusetts, United States

Full record on ClinicalTrials.gov

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