Acute Comfort and Blur Profile of a Lubricant Eye Drop Versus a Marketed Eye Ointment

Alcon

Status: Completed

Conditions: Dry Eye

Treatments: Other: Lubricant eye drop FID 115958D; Other: Refresh PM Ointment

Study type: Interventional

Funder types: Industry

Identifiers

NCT01076998

C-09-059

Details and patient eligibility

About

The purpose of this study is to compare the comfort and blurriness of the investigational lubricant eye drop with a marketed artificial tear ointment.

Enrollment: 24 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Documented diagnosis of dry eye

Exclusion criteria

• Must not have worn contact lenses within 12 hours preceding enrollment
• Must not have used any topical ocular drops or ointment within 24 hours preceding enrollment

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Triple Blind

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24 participants in 2 patient groups

Lubricant eye drop

Experimental group

Description:

Lubricant eye drop

Treatment:

Other: Lubricant eye drop FID 115958D

Refresh PM Ointment

Active Comparator group

Description:

Refresh PM Ointment

Treatment:

Other: Refresh PM Ointment