ISRCTN74288501已完成不适用
ong-term safety, effectiveness and clinical experience of the CyPass glaucoma implant when used in the standard clinical environment: a multicentre registry study with retrospective and/or prospective data capture
Transcend Medical, Inc.™ (USA)0 个研究点目标入组 500 人开始时间: 2010年6月17日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 500
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
- 性别
- All
入选标准
- •1. Able to understand study requirements and willing to follow study instructions and provide written consent
- •2. Diagnosis of glaucoma in the study eye
- •3. At the preoperative visit, a mean medicated or unmedicated intraocular pressure (IOP) in the study eye of greater than or equal to 18 mmHg and less than or equal to 44 mmHg
排除标准
- •1. Diagnosis of acute angle closure, narrow angle, uveitic or neovascular glaucoma in the study eye
- •2. Diagnosis of normal tension glaucoma in the study eye
研究者
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