JPRN-jRCT2032200147已完成3 期
Clinical Investigation of AcrySof IQ PanOptix Toric Intraocular Lens Model TFNT20
Bissen-Miyajima Hiroko0 个研究点目标入组 32 人开始时间: 2020年10月12日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 32
研究概览
简要总结
The primary endpoint of this study was the percentage of eyes with <=0.25 D cylinder power at 1-2 months postoperative. The percentage of eyes with <=0.25 D of absolute refractive cylinder was 90.2% at Visit 3/3A (Day 30-60), showing a significant difference from the historical threshold calculated based on the past studies using non-toric IOLs. No AEs related to the study device were reported. No subjects discontinued the study due to AEs, and there were no safety concerns of the study device.
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 20age old 至 ot applicable(—)
- 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.
研究者
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