jRCT2032200147已完成不适用
Clinical Investigation of AcrySof IQ PanOptix Toric Intraocular Lens Model TFNT20
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 32
- 主要终点
- -
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomized Controlled Trial
- 干预模型
- Single Assignment
- 主要目的
- Treatment Purpose
- 盲法
- Open(masking Not Used)
入排标准
- 年龄范围
- 20age old over 至 No limit（—）
- 性别
- All
入选标准
- •Eligible to be implanted with AcrySof IQ PanOptix Toric Intraocular Lens Model TFNT20 in at least one eye as determined by a new Alcon Toric calculator.
- •Planned postoperative emmetropia (spherical equivalent +-0.50 D).
- •Other protocol-specified inclusion criteria may apply.
排除标准
- •Irregular corneal astigmatism.
- •History of anterior segment (corneal, anterior chamber, sulcus) or posterior segment (uveal, vitreo-retinal) pathology.
- •Glaucoma; ocular hypertension; diabetic retinopathy; any optic nerve pathology.
- •History of previous intraocular or corneal (refractive or trauma related) surgery.
- •Any other planned ocular surgical procedures including but not limited to limbal relaxing incision (LRI)/Astigmatic Keratotomy and LASIK.
- •Other protocol-defined exclusion criteria may apply.
结局指标
主要结局
-
Percentage of eyes with <= 0.25 diopter (D) refractive cylinder at Visit 3/3A (Day 30-60).
次要结局
- Percentage of eyes with <= 0.5 D refractive cylinder(Visit 3/3A (Day 30-60))
- Average manifest refractive cylinder(Visit 3/3A (Day 30-60))
研究者
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