ISRCTN16769682进行中（未招募）Unknown
An observational, registry-based study of performance and safety data from participants treated for open angle glaucoma or ocular hypertension with the Eagle device
BELKIN Vision Ltd.0 个研究点目标入组 550 人开始时间: 2024年7月2日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 550
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
- 性别
- All
入选标准
- •1. Adult participants who underwent treatment with the Eagle device for treatment of Open Angle Glaucoma including exfoliative or pigmentary glaucoma or ocular hypertension as per the approved indication.
- •2. Participants with expected post-operative follow-up data of at least six (6) months
排除标准
- •Records of participants with any of the following conditions at the date of the treatment with the Eagle device, will not be included in the data collection:
- •1. Participants who are unable to fixate their head and/or eyes, such as participants suffering from nystagmus, tremors or similar conditions.
- •2. Participants with congenital glaucoma or active anterior segment inflammations.
- •3. Participants with any condition that obscures the limbus, such as melanosis affecting the limbus, severe arcus senilis affecting the limbus, pterygium affecting the limbus or any other such conditions.
- •4. Participants with any condition that causes poor visualization of the limbus that prevents the Eagle device’s treatment target identification.
研究者
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