24-hour Efficacy and Tolerability of the Tafluprost-timolol Fixed Association Without Preservatives in Glaucomatous or Ocular Hypertensive Patients Already Treated With Latanoprost Preserved With BAK. A Prospective, Open Study of 3 Months Duration.
试验速览
- 阶段
- 4 期
- 发起方
- 入组人数
- 43
- 试验地点
- 3
- 主要终点
- The evaluation of the mean 24-h absolute Intraocular Pressure (IOP)
研究概览
简要总结
This is a phase IV, interventional, multi-center, open clinical Trial. Patients will be administered one eye drop of tafluprost/timolol fixed combination at 20:00 (+/- 1 hour), in the treatment of open angle glaucoma and ocular hypertension. The patients will suspend the treatment with latanoprost.
详细描述
This is a phase IV, interventional, multi-center, not comparative, open clinical Trial to evaluate the effectiveness in reducing the mean 24-hour IOP of the preservative-free fixed combination of Tafluprost 0.0015% and Timolol 0.5% administered once at night (8pm) in POAG or OHT patients suffering from mild OSD and requiring further IOP reduction while in topical treatment with BAK-preserved Latanoprost 0.05 mg/ml. Three Italian recruiting centers are included in the study and the estimated number of patients to be enrolled is 43. After evaluating the patient's eligibility, the patients will suspend the treatment with latanoprost and will be administered one eye drop of tafluprost/timolol fixed combination at 20:00 (+/- 1 hour) at the end of the V1B visit. Active drug will be contained (about 30 µl, one drop) contains about 0.45 micrograms of tafluprost and 0.15 mg of timolol.
The Study consists in 6 Visits:
- Screening visit V0 and baseline V1A.
- Treatment period visit V1B; V2; V3A; V3B.
- End of study V3B.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 盲法
- None
盲法说明
Open label
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Ocular hypertension or primary open-angle glaucoma or secondary to dispersion of pigment or pseudoesfoliatio;
- •IOP <22 mmHg in latanoprost therapy in both eyes since at least 6 weeks and > 17 mmHg in at least one eye;
- •OSD at least mild as defined by DEQ-5 (score> 6);
- •Examination of the visual field during the three months prior to enrollment (if not present, the patient must be subjected to a visual field at the screening visit);
- •Treatment with latanoprost BAK-preserved from at least 6 weeks;
- •Subject agrees to follow the study procedures and signs the EC-approved ICF;
- •For women of child-bearing potential, blood screening for beta-HCG before randomization and use of one effective method of birth control during the conduct of the study
排除标准
- •Inability to understand and sign informed consent;
- •Age under 18 years;
- •Other forms of secondary glaucoma (besides pigmentary and pseudoesfoliatius);
- •Narrow angle or history of acute glaucoma attacks;
- •Previous history of trabeculoplasty in the previous 6 months;
- •History of glaucoma surgery or refractive surgery;
- •Cataract surgery in the 6 months prior to enrollment;
- •Contraindications to the use of beta-blockers (reactive airway disease, including bronchial asthma or a history of bronchial asthma, severe chronic obstructive pulmonary disease; sinus bradycardia, sick sinus syndrome, including sinoatrial block, second or third degree atrioventricular block not controlled by pacemaker; full-blown heart failure, cardiogenic shock);
- •Damage to the visual field with a mean deviation (MD) <-20 dB;
- •BCVA <2/10;
- •Topical ocular drugs performed within 3 months prior to enrollment that may interfere with the study results (eg steroids, non-steroidal anti-inflammatory drugs, immunosuppressants, etc.);
- •Use of tear substitutes containing preservatives within 30 days prior to enrollment;
- •Any other condition that, in the opinion of the investigator, may compromise the safety or compliance of the patient or would preclude the patient from successful completion of the study or would impair interpretation of results;
- •Corneal anomalies that preclude an accurate measurement of IOP (eg astigmatism> 3 D, keratoconus, opacity or corneal ulcers);
- •Any type of previous corneal or conjunctival surgery including pterygium removal or refractive surgery;
- •Unstable systemic disorders that may require the initiation or variation of therapies that may influence intraocular pressure during the study;
- •Woman of childbearing potential, or who is currently pregnant or breastfeeding;
- •Inability to adhere to the procedures required by the protocol or to the studio treatment;
- •Participation in another experimental therapeutic protocol within one month prior to baseline and during the study period (participation in natural history study is allowed);
- •Hypersensitivity to the active substances or to any of the excipients.
研究组 & 干预措施
tafluprost/timolol
Enrolled patients will be treated with one drop of the fixed combination Tafluprost-Thymol without preservative in the evening at 20.00 (+/- 1 hour). Patients will be administrered with one drop in the conjunctival sac of the affected eye (s) once a day.
干预措施: tafluprost/timolol (Drug)
结局指标
主要结局
The evaluation of the mean 24-h absolute Intraocular Pressure (IOP)
时间窗: through study completion, an average of 3 months
Reduction measured in mmHg (millimeters of mercury).
次要结局
- Evaluation of the changes in the Corneale Staining Test (CFS) and Break-up Time Test (tBUT) parameters(through study completion, an average of 3 months)
- Evaluation of the changes of the number of conjunctival goblet cells to confocal microscopy(through study completion, an average of 3 months)
- Evaluation of the average reduction of Intraocular Pressure(IOP) at 24-hour(through study completion, an average of 3 months)
- Evaluation of the changes of the number, activation of corneal, conjunctival dendritic cells to confocal microscopy.(through study completion, an average of 3 months)
- Evaluation of the changes in quality of life(through study completion, an average of 3 months)
- Evaluation of the percentage reduction of the average Intraocular Pressure(IOP) of the 24 hours(through study completion, an average of 3 months)
- Evaluation of the percentage of patients achieving Intraocular Pressure(IOP) reduction in average(through study completion, an average of 3 months)
- Evaluation of the average daytime reduction and night of the Intraocular Pressure(IOP)(through study completion, an average of 3 months)
- Evaluation of the changes in Dry Eye Questionnaire (DEQ-5)(through study completion, an average of 3 months)