CTRI/2016/06/007001已完成4 期
TO COMPARE THE EFFECT OF BENZALKONIUM CHLORIDE-PRESERVED LATANOPROST AND BENZALKONIUM CHLORIDE-FREE LATANOPROST ON OCULAR SURFACE HEALTH IN PATIENTS OF PRIMARY OPEN ANGLE GLAUCOMA OR OCULAR HYPERTENSIO
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 30
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
- •Established cases of POAG or ocular hypertension with IOP controlled on monotherapy of BKC-preserved latanoprost for more than three months.
排除标准
- •1 Known lack of ocular hypotensive response to topical ophthalmic, prostaglandin analogs (in the opinion of the investigator).
- •2 Intraocular conventional surgery or laser surgery within the past one year.
- •3 Any refractive surgery in study eye .
- •4 Patients on steroids medication.
- •5 Ocular trauma within the past 3 months.
- •6 Patients suffering from Rheumatoid arthritis or any other systemic disease which also causes dry eye.
- •7 Patients taking any other medication which also causes dry eye.
- •8 Progressive retinal or optic nerve disease apart from glaucoma.
- •9 Concurrent infectious/non infectious conjunctivitis, keratitis, or uveitis in either eye.
- •10 Any abnormality preventing stable applanation tonometry.
- •11 Use of contact lens for the duration of the study.
- •12 Any opacity or subject uncooperativeness that restricts adequate examination of the ocular fundus or anterior chamber.
- •13 Clinically significant ocular disease (e.g., corneal edema, uveitis, severe keratoconjunctivitis sicca) which might interfere with the study,.
- •14 Clinically significant systemic disease which might interfere with the study.
- •15 History of non-compliance to medical regimens or unwilling to comply with the study protocol.
- •16 Patients with hypersensitivity or poor tolerance to any components of the study medication.
- •17 Angle closure glaucoma or a history of acute angle closure treated with a peripheral iridotomy.
- •18 Participation in another clinical study within the last thirty (30) days.
研究者
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