Tear Film Break-Up Time Evaluation of FID 114657

Alcon

Status: Completed

Conditions: Dry Eye

Treatments: Other: FID114657; Other: SootheXP Emollient (Lubricant) Eye Drops

Study type: Interventional

Funder types: Industry

Identifiers

NCT01023464

C-09-030

Details and patient eligibility

About

To evaluate the effects of FID 114657 on tear film break-up time in dry eye patients.

Enrollment: 38 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. The informed consent document and HIPAA privacy document must be read, signed and dated by the patient or legally authorized representative before conducting any procedures.
2. Patients (minimum age 18) with dry eye. Criteria for the diagnosis must include the following characteristics at Visit 1 (Screening): Patients' 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 <5 seconds in at least one eye; > Grade 1 for Meibomian Gland Expression in both eyes; Evidence of missing meibomian glands in both eyes.
3. Able and willing to follow study instructions.
4. Patients must have best-corrected visual acuity of 0.6 logMAR or better in each eye as assessed using an ETDRS chart at Visit 1.
5. Patients must not have used any topical ocular drops for approximately 24 hours prior to Visit 1.

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 of intolerance or hypersensitivity to any component of the study medications.
5. 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.
6. Use of any concomitant topical ocular medications during the study period.
7. Patients using systemic medications that may contribute to dry eye (e.g. cold and allergy medications, tricyclic antidepressants, hormone replacement therapies) may not be enrolled in the study unless they have been on a stable dosing regimen for a minimum of 30 days prior to Visit 1. In addition, the dosing regimen must remain stable throughout the study.
8. Ocular conditions such as conjunctival infections, iritis, or any other ocular condition that may preclude safe administration of the test article.
9. Individuals unwilling to discontinue contact lens wear during the study period. Contact lens wear must have been discontinued at least one week prior to Visit 1.
10. Enrollment of investigator's office staff, relatives, or members of their respective households; or enrollment of more than one member of the same household.
11. Participation in an investigational drug or device study within 30 days of entering this study.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Double Blind

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38 participants in 2 patient groups

Period 1

Other group

Description:

FID 114657 or SootheXP

Treatment:

Other: FID114657

Other: SootheXP Emollient (Lubricant) Eye Drops

Period 2

Other group

Description:

FID 114657 or SootheXP

Treatment:

Other: FID114657

Other: SootheXP Emollient (Lubricant) Eye Drops