An evaluation of the Ocular Surface Health in Subjects Using DuoTrav APS Eye Drops Solution Versus XALACOM® EYE Drops Solutio

Conditions: glaucoma/dry eye
MedDRA version: 9.1Level: LLTClassification code 10030348Term: Open angle glaucoma
MedDRA version: 9.1Level: HLGTClassification code 10018307Term: Glaucoma and ocular hypertension
MedDRA version: 9.1Level: LLTClassification code 10030043Term: Ocular hypertension
MedDRA version: 9.1Level: LLTClassification code 10013774Term: Dry eye

Registration Number: EUCTR2009-010604-29-HU

Lead Sponsor: Alcon Research, Ltd.

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: ot Recruiting

Sex: All

Target Recruitment: 700

Inclusion Criteria

1. Patients = 18 years of age.
2. Must have a clinical diagnosis of open-angle glaucoma (with or without pseudoexfoliation or pigment dispersion component), or ocular hypertension in at least one eye.
3. Ocular Surface Disease Index (OSDI) score of = 13.
4. Must have a corneal fluorescein staining score of = 1 in at least one eye
5. Must have had their IOP controlled using only the fixed combination XALACOM® for at least 1 continuous month immediately prior to Visit 1 in at least one eye.
6. The intraocular pressure should be able to be controlled in the opinion of the investigator and stable while on fixed combination with the study medication for the eye(s) currently being dosed with XALACOM®.
7. Must have an intraocular pressure in both eyes that, in the opinion of the investigator, is considered to be stable and safe for the patient.
8. The last dose of XALACOM® must have been instilled within 24 hours of Visit 1.
9. Must be willing and able to discontinue use of any topical ocular medication other than the study medication for the duration of the study.
10. Best-corrected visual acuity score of = 55 ETDRS letters read in each eye
11.Women of childbearing potential must meet all of the following conditions at Visit 1:
• They are not breast-feeding.
• They have a negative urine pregnancy test at Visit 1.
• They agree to undertake a urine pregnancy test upon entering and exiting the study.
• They are not planning to become pregnant during the course of the study.
• They are currently using, and agree to continue to use adequate birth control methods for the duration of the study. Adequate birth control methods are defined as:
Hormonal: oral, implantable, topical, or injectable contraceptives
Mechanical: IUD, spermicide in conjunction with a barrier such as condom or diaphragm
Surgical: sterilization of partner and / or self
Abstinence: If patients become sexually active, they must agree to use one of the birth
control methods (hormonal, mechanical, or surgical) listed above.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

1. Any abnormality preventing reliable applanation tonometry in the study eye(s).
2. Presence of any ocular pathology in either eye seen during the slit lamp or fundus exams, that in the opinion of the investigator may preclude the safe administration of test article or safe participation in this study.
3. Dry eye or KCS which has been, or is currently being, treated with the use of punctal plugs, punctal cautery, Restasis®, or topical ocular corticosteroids.
4. Patients who have undergone keratorefractive ocular laser procedures, corneal surgery or surgery to the corneal surface, including but not limited to LASIK and PRK, within 1 year prior to Visit 1.
5. Any other ocular laser surgery in either eye within 3 months prior to Visit 1.
6. Patients who have undergone intraocular or extra-ocular surgery, in either eye, within 6 months prior to Visit 1.
7. History of progressive retinal or optic nerve disease other than glaucoma.
8. Severe central visual field loss in either eye based upon the clinical judgment of the investigator.
9. Any history of, or current evidence of, infectious or inflammatory ocular conditions, such as clinically significant blepharitis in the past 2 years, rosacea affecting the eye adnexa and its ocular sequelae (e.g., hordeola, chalazion, recurrent meibomian gland dysfunction), clinically significant corneal dystrophies, recurrent inflammatory eye diseases (e.g., uveitis, scleritis, herpes keratitis, iritis, etc), ocular allergies known to occur during the season in which the patient is enrolled in this study.
10. Ocular trauma within 6 months prior to Visit 1 in either eye, as determined by patient history and/or examination.
11. History or evidence of corneal transplant or transplant variant procedures [Descemet’s stripping endothelial keratoplasty (DSEK), Descemet’s stripping endothelial automated keratoplasty (DSAEK), lamellar keratoplasty, etc.].
12. Patients with suspected or diagnosed Sjogren’s syndrome.
13. History of or current bronchial asthma, or severe chronic obstructive pulmonary disease that would preclude the safe administration of a topical beta-adrenergic blocking agent.
14. History of or current severe, unstable or uncontrolled cardiovascular, hepatic, or renal disease (e.g., sinus bradycardia, overt cardiac failure, greater than first degree
atrioventricular block, cardiogenic shock, clinically relevant angina or uncontrolled
hypertension) that would preclude the safe administration of a topical beta-adrenergic blocking agent.
15. History of spontaneous or current hypoglycemia or uncontrolled diabetes.
16. History of or current severe allergic rhinitis and bronchial hyper reactivity.
17. History of intolerance or hypersensitivity to any component of the test articles.
18. Use of any systemic medications on a chronic basis that have not been on a stable dosing regimen for at least 30 days prior to Visit 1, or an anticipated change in dosing regimen of medications during the course of the study.
19. Use of ocular medications (including over the counter and prescription medications) other than XALACOM® within 7 days of Visit 1.
20. Use of corticosteroids within 30 days of Visit 1, or any anticipated use of corticosteroids during the course of the study.
21. Use of contact lenses within 30 days of Visit 1. Concomitant use of contact lenses is also excluded for the duration of the study.
22. Participation in an investigational drug or device study within 30 days of entering this study.

Study & Design

Study Type: Interventional clinical trial of medicinal product

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method

Secondary Outcome Measures

Name	Time	Method

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