Glaucoma, Open-Angle
Conditions
Keywords
tafluprost/timolol fixed combination, 24-hour IOP control
Brief summary
The ideal dosing for preservative-free tafluprost/timolol fixed combination remains to be elucidated. The present study compared the 24-hour intraocular pressure efficacy obtained with tafluprost/timolol given once in the evening with placebo once in the morning, versus that with the same fixed combination administered once in the morning with placebo given once in the evening in consecutive patients with open-angle glaucoma insufficiently controlled with branded, or generic latanoprost monotherapy.
Detailed description
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 1. Mean efficacy with the evening dosing of tafluprost/timolol compared with the morning-dosed tafluprost/timolol fixed combination at each time point measured. 2. Mean daytime and mean nighttime IOP control with the two dosing regimens. 3. Mean peak and fluctuation of 24-hour pressure with the evening and the morning dosing of the fixed combination.
Interventions
DRUGTafluprost/timolol fixed combination
Evaluation of 24-hour pressure control with tafluprost/timolol given in the evening or morning
Sponsors
Santen Oy
Aristotle University Of Thessaloniki
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)
Masking description
Only the dosing coordinator is aware of the treatment used.
Intervention model description
Patients first undergo a baseline, habitual 24-hour pressure assessment with branded, or generic latanoprost. Suitably qualified open-angle glaucoma patients (latanoprost-treated, mean 24-hour pressure greater than 20 mm Hg) are randomized for Period 1 to receive either tafluprost/timolol fixed combination drops once in the evening (20:00) and placebo drops in the morning (08:00), or tafluporst/timolol drops once in the morning (08:00) and placebo in the evening (20:00). After 3 months of chronic therapy (± 2 weeks) study patients undergo a treated, habitual 24-hour pressure assessment. Study subjects are then switched to the opposite treatment regimen for Period 2 (tafluprost/timolol in the evening instead of morning etc) and after another 3 months they undergo the third and final evaluation of their 24-hour pressure.
Eligibility
Sex/Gender
ALL
Age
21 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
1. age between 21-85 years; 2. 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); 3. visual acuity greater than 0.1 in the study eye; 4. open anterior chamber angles; 5. in each patient the diagnosis of open-angle glaucoma will be made by the principal investigator based on the European Glaucoma Society criteria; 6. 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); 7. 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
1. previous history of less than 10% IOP decrease on any IOP-lowering medication; 2. evidence of concurrent conjunctivitis, keratitis, or uveitis in either eye; 3. history of inadequate adherence; intolerance, or contraindication to either prostaglandins, β-blockers, dorzolamide, or benzalconium chloride (BAK); 4. severe ocular surface disease, intraocular conventional or laser surgery in the study eye (within 6 months prior to enrolment); 5. previous history of ocular trauma; 6. use of corticosteroids (within 3 months before the enrolment) and use of contact lenses; 7. 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; 8. unwillingness to participate in the trial; 9. females of childbearing potential or lactating mothers.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Mean 24-hour pressure control with Tafluprost/timolol fixed combination dosed morning or evening | 3-month study | 24-hour efficacy documented after each period of therapy |
Countries
Greece
Outcome results
None listed