Preservative-free Tafluprost/Timolol Fixed Combination: Morning vs Evening Dosing

Prospective, observer-masked, placebo-controlled, crossover, comparison in consecutive open-angle glaucoma patients, insufficiently controlled with preserved latanoprost monotherapy (mean 24-hr IOP greater than 20 mmHg). Patients were randomized to either morning (08:00), or evening (20:00) preservative-free tafluprost/timolol fixed combination for 3 months and then were crossed over. After each treatment period patients underwent habitual 24-hour intraocular pressure monitoring with Goldmann tonometry in the sitting position (at 10:00, 14:00, 18:00 and 22:00) and Perkins tonometry in the supine position (at 02:00 and 06:00).

Primary Study Objective: Mean 24-hour efficacy with both dosing regimens of tafluprost/timolol fixed combination versus latanoprost monotherapy.

Secondary Study Objectives

• Mean efficacy with the evening dosing of tafluprost/timolol compared with the morning-dosed tafluprost/timolol fixed combination at each time point measured.
• Mean daytime and mean nighttime IOP control with the two dosing regimens.
• Mean peak and fluctuation of 24-hour pressure with the evening and the morning dosing of the fixed combination.

Inclusion criteria

• age between 21-85 years;
• mild to moderate glaucomatous disc damage and visual field loss (less than -12 dB mean deviation visual field loss attributed to glaucoma and 0.8 or better vertical cup-to-disc ratio);
• visual acuity greater than 0.1 in the study eye;
• open anterior chamber angles;
• in each patient the diagnosis of open-angle glaucoma will be made by the principal investigator based on the European Glaucoma Society criteria;
• study patients will have to demonstrate a reliable visual field (at least two visual fields with less than 20% fixation losses, false positives, or negatives);
• patient should understand the study instructions and to be willing to attend all follow-up appointments and should be willing to comply with study medication usage.

Exclusion criteria

• previous history of less than 10% IOP decrease on any IOP-lowering medication;
• evidence of concurrent conjunctivitis, keratitis, or uveitis in either eye;
• history of inadequate adherence; intolerance, or contraindication to either prostaglandins, β-blockers, dorzolamide, or benzalconium chloride (BAK);
• severe ocular surface disease, intraocular conventional or laser surgery in the study eye (within 6 months prior to enrolment);
• previous history of ocular trauma;
• use of corticosteroids (within 3 months before the enrolment) and use of contact lenses;
• patients will also be excluded if on baseline exam they show clinical evidence of inflammation, signs of ocular infection (except blepharitis), signs of any corneal abnormality that will affect subsequent IOP measurements;
• unwillingness to participate in the trial;
• females of childbearing potential or lactating mothers.