TCTR20210219002尚未招募4 期
Efficacy of 0.28 % Sodium hyaluronate eyedrop in patient with evaporative dry eye in Rajavithi Hospital: randomized double-blind controlled trial.
ational innovation agency, Thailand0 个研究点目标入组 50 人开始时间: 2021年2月19日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 50
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
- 年龄范围
- 18 Years 至 N/A (No limit)（—）
- 性别
- All
入选标准
- •Age more than 18 years.
- •Ocular surface disease Index not more than 13
- •Noninvasive tear break up time less than 10 seconds, both eyes.
- •Schirmer 1 test more than 5.5 mm. (in 5 minutes), both eyes.
排除标准
- •Oxford grading scale not more than 4
- •Previous preservative eye drop use in 1 week.
- •Previous ocular surgery in 4 months.
- •History of nasolacrimal duct obstruction.
- •Allergy to sodium hyaluronate.
- •History of other ocular disease for example glaucoma, uveitis.
- •History of contact lenses used.
- •History of use connective tissue disease for example rheumatoid arthritis SLE, Sjogren disease.
研究者
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