Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Fort Worth, Texas 76134


Purpose:

The primary objective of this investigation will be to quantify the increase in tear film break-up time (TFBUT) associated with the instillation of a single eyedrop of an Ocular Emulsion in dry eye sufferers.


Study summary:

The secondary objective of this investigation will be to compare the tear film break up time measured with two different techniques.


Criteria:

Inclusion Criteria: 1. The subject must be 18 years of age or older; 2. The subject must have a best corrected visual acuity of 0.6 LogMAR (~6/24) or better in each eye 3. The subject must not have used any topical ocular drops for approximately 24 hours prior to the enrolment/screening visit 4. The subject must be classified as dry eye at enrolment/screening visit according to the following criteria: - Subjects' self-assessment of dry eye status (answer of at least "some of the time" to the question, "How often have your eyes felt dry enough to want to use eye drops?"); - TFBUT measured with DET ≤ 5 seconds in at least one eye; - Grade 1 for meibomian gland expression in both eyes; - Evidence of missing meibomian glands in both eyes. Exclusion Criteria: 1. History or evidence of ocular or intraocular surgery in either eye within the past six months. 2. History or evidence of serious ocular trauma in either eye within the past six months. 3. Current punctal occlusion of any type (e.g., collagen plugs, silicone plugs). 4. History or evidence of epithelial herpes simplex keratitis (dendritic keratitis); vaccinia; active or recent varicella viral disease of the cornea and/or conjunctiva; chronic bacterial disease of the cornea and/or conjunctiva and/or eyelids; mycobacterial infection of the eye; and/or fungal disease of the eye. 5. Use of any concomitant topical ocular medications during the study period. 6. Ocular conditions such as conjunctival infections, iritis, or any other ocular condition that may preclude the safe administration of either drop under investigation. 7. Participation in an investigational drug or device study within 30 days of entering this study.


NCT ID:

NCT01368198


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Fort Worth, Texas 76134
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.