Comparative Study of Rohto Dry-Aid® and Systane® Ultra in Patients With Dry Eye

Completed · Phase 4

Conditions studied: Dry Eye Syndromes, Dry Eye

In brief

The objective of this study is to evaluate the efficacy of Rohto Dry-Aid® in comparison to Systane® Ultra on visual function and tear film stability in patients diagnosed with Dry Eye.

Key facts

Study ID

NCT03183089

Run by

The Mentholatum Company

People needed

80

Starts

2015-12-03

Expected to finish

2016-01-04

Last updated by the study team

2017-06-09

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Be at least 18 years of age
• Provide written informed consent
• Have a reported history of dry eye
• Have a history of use of eye drops for dry eye symptoms
• Ocular discomfort
• Conjunctival redness
• Tear film break up time
• Corneal and Conjunctival Staining

You may not qualify if…

• Have any clinically significant slit lamp findings at entry visit
• Be diagnosed with an ongoing ocular infection
• Have any planned ocular and/or lid surgeries over the study period
• Have an uncontrolled systemic disease
• Be a woman who is pregnant, nursing or planning a pregnancy
• Be a woman of childbearing potential who is not using an acceptable means of birth control
• Have a known allergy and/or sensitivity to the test article or its components
• Have a condition or be in a situation which the investigator feels may put the subject at significant risk, may confound the study results, or may interfere significantly with the subject's participation in the study

Where it is running

• Andover Eye Associates — Andover, Massachusetts, United States

Full record on ClinicalTrials.gov

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