CTRI/2015/10/006320Other3 期
Clinical Evaluation of Systane® Balance on Corneal Staining in Indian Subjects with Dry Eye
Alcon laboratories India pvt Ltd0 个研究点目标入组 14 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- Other
- 发起方
- 入组人数
- 14
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. Sign Informed Consent and willing and able to attend all study visits
- •2. Dry eye in both eyes diagnosed by an ophthalmologist
- •3. Other protocol-specified inclusion criteria may apply
排除标准
- •1. Women of childbearing potential who are pregnant or breast feeding.
- •2. Any medical condition (systemic or
- •ophthalmic) that may preclude the safe
- •administration of test article or safe participation in the study
- •3. Ocular surgery or ocular trauma requiring medical or pharmacological treatment
- •within 1 year of Screening
- •4. Use of topical ocular prescription or non-prescription medications, RESTASIS or topical ocular steroids within 14 days of screening
- •5. Use of any artificial tears/gels/lubricants/rewetting drops within 4 hours of screening
- •6. Contact lens wear within 1 week of Screening and/or unwillingness to discontinue contact lens wear for the duration of the study
- •7. Other protocol-specified exclusion criteria may apply
研究者
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