ISRCTN64155646已完成未知
Evaluation of post-operative dysphotopsia and spectacles independence after bilateral multifocal intraocular lens (IOL) implantation for cataract surgery and refractive lens exchange: Acri.LISA® 366D versus AcrySof® SN6AD1 randomised clinical trial
Moorfields Eye Hospital NHS Foundation Trust (UK)0 个研究点目标入组 188 人开始时间: 2010年9月6日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 188
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. Patients undergoing sequential bilateral cataract surgery or refractive lens exchange
- •2. Patients that want to be spectacle independent
- •3. Male or female, aged 21 years and above
排除标准
- •1. Any significant ocular co-morbidity (amblyopia, age-related macular degeneration [ARMD], glaucoma, etc) precluding post-operative visual acuity (VA) of 20/30 or better or poor zonular/capsular stability (e.g. after trauma/severe pseudoxanthoma elasticum [PXE])
- •2. Corneal astigmatism more than 1.50 D on IOLMaster keratometry. Corneal astigmatism between 1.00 - 1.50 D will be reduced using standardised limbal relaxing incisions (LRI).
- •3. IOLMaster biometry not possible
- •4. IOL power less than 10D or greater than 30D
- •5. Professional night drivers, pilots, and other occupations for which induced
- •dysphotopsia may be career threatening
- •6. Patients with severe psychiatric disorders
- •7. Vulnerable groups
- •8. Poor mobility
- •9. Poor comprehension of written English
研究者
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