CTRI/2024/06/068514尚未招募4 期
A post market clinical follow up prospective study to evaluate safety and performance of Sodium Hyaluronate Ophthalmic Solution - NI
Kilitch Healthcare India Ltd.0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •Subjects who are able to give voluntary, written informed consent to participate in this study.
- •Subjects who experience eye dryness, eye soreness/ burning, irritative sensation and discomfort
- •of eyes due to the continuous use of computer/ TV/ exposed pollution/ dry environment.
排除标准
- •Anyone with known allergic reaction to Sodium Hyaluronate Ophthalmic Solution.
- •Subjects with existing eye infection.
- •History of ocular surgery. History or active signs of severe or serious ocular conditions such as
- •inflammatory corneal ulcers, recurrent erosions, and uveitis at any time.
- •Patients participating in any another clinical trial during study.
研究者
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