A 3-month Study Investigating the 24-hour Efficacy With the Preservative-free Tafluprost/Timolol Fixed Combination Dosed Morning, or Evening in Subjects With Open-angle Glaucoma Insufficiently Controlled With Latanoprost Monotherapy
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 42
- 试验地点
- 1
- 主要终点
- Mean 24-hour pressure control with Tafluprost/timolol fixed combination dosed morning or evening
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Single (Investigator)
盲法说明
Only the dosing coordinator is aware of the treatment used.
入排标准
- 年龄范围
- 21 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •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.
排除标准
- •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.
研究组 & 干预措施
Tafluprost/timolol with PM dosing
Therapy with Tafluprost/timolol fixed combination drops dosed PM (20:00)
干预措施: Tafluprost/timolol fixed combination (Drug)
Tafluprost/timolol with AM dosing
Therapy with Tafluprost/timolol fixed combination drops dosed AM (08:00)
干预措施: Tafluprost/timolol fixed combination (Drug)
结局指标
主要结局
Mean 24-hour pressure control with Tafluprost/timolol fixed combination dosed morning or evening
时间窗: 3-month study
24-hour efficacy documented after each period of therapy
次要结局
未报告次要终点
研究者
AGP Konstas
Professor in Ophthalmology
Aristotle University Of Thessaloniki