CTIS2023-504173-21-00进行中（未招募）1 期
MyKid-study: efficacy and systemic side effects of intracameral Mydrane® injections in children undergoing cataract surgery. - EDGE1169
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 40
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
- 0 至 17（—）
- 性别
- All
入选标准
- •Children aged 8 weeks to 17 years old who are scheduled for surgical cataract repair of one or both eyes
排除标准
- •Patients with a reported allergy for one of the components of Mydrane®, Patients younger than 8 weeks, patients who previously had cataract surgery of one eye within this study and receive surgery of the contralateral eye on a different day, Patients who are pregnant. Girls of childbearing age will be tested for pregnancy with urinary analysis (hCG) at the time of inclusion
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