CTRI/2018/03/012724已完成未知
A Randomized, Open-Label, Parallel Comparative Trial on Efficacy and Safety of the Fixed Vs Unfixed Combination of Latanoprost and Timolol in Patients of Open-Angle Glaucoma and Ocular Hypertension Insufficiently Controlled on Timolol and Latanoprost Monotherapy.
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 80
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Patients 18 years of age of either sex with primary open angle glaucoma or ocular hypertension.
- •Patients receiving either latanoprost 0.005% once daily or either timolol 0.5% once or twice daily in the preceding four weeks.
- •Patients with IOP >21 mmHg not controlled with prior monotherapy of latanoprost or timolol.
排除标准
- •Patients with age <18 years of age.
- •Patients with acute angle closure glaucoma
- •Patients with hypersensitivity to either of the two drugs.
- •Patients having co-morbid conditions like CHF, history of conduction defect or cardiogenic shock, heart block, COPD/asthma, angina, acute/uncontrolled medical or psychiatric illness, pregnancy/lactation, ocular inflammation/ocular infection and myasthenia gravis.
- •Patients with normotensive glaucoma.
研究者
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