CTRI/2010/091/001459已完成3 期
A Comparative, Randomized, Double Blind, Multicentric, Prospective Clinical Study to evaluate the efficacy, safety and tolerability of Tafluprost Ophthalmic solution 15 mcg/ml Vs. Latanoprost eye drops 0.005 % in patients with Glaucoma.
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 200
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
- •1.Patients with diagnosis of glaucoma.
排除标准
- •Pregnant or nursing females.
- •Patients with exfoliation glaucoma and neovascular glaucoma.
- •Patients with diabetic retinopathy.
- •Patients with advanced visual field loss (MD <-15dB).
- •Excessive myopia (<-6D).
- •Any corneal abnormality or other condition preventing reliable applanation tonometry.
- •Presence of any external disease and inflammation of the eye.
- •History of refractive surgery.
- •History of laser trabeculoplasty, filtering surgery, trabeculotomy, cataract surgery, and other intraocular surgery.
研究者
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