CTRI/2011/06/001845已完成3 期
Clinical Evaluation of an Investigational contact lens in 7-Day Extended Wear - NI
Johnson and Johnson Vision Care Inc0 个研究点目标入组 85 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 85
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
- •A.Be between 18 and 39 years of age.
- •B.Require a visual correction in both eyes (Monovision not allowed)
- •C.Require a soft contact lens spherical correction between -0.50 and -5.75D in both eyes.
- •D.Have an astigmatic correction less than 1.50D in both eyes.
- •E.Be able to regularly wear the lenses on a 7 day/6 night extended wear basis (e.g. does not regularly swim more than once a week)
- •F.Be correctable to a visual acuity of 20/30 or better in each eye with spherical distance correction.
- •G.Have normal eyes with no evidence of abnormality or disease.
排除标准
- •A.Requires concurrent ocular medication.
- •B.Any systemic illness which would contraindicate lens wear or the medical treatment of which would affect vision or successful lens wear.
- •C.Clinically significant (Grade 3 or 4) slit lamp findings including corneal edema, corneal vascularization, corneal staining, tarsal abnormalities, bulbar injection, or any other abnormality of the cornea that would contraindicate contact lens wear.
- •D.Is currently or has previously worn any hard PMMA or RGP contact lenses.
- •E.Known hypersensitivity to silver, silver ions or silver containing compounds.
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