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临床试验/NCT04875455
NCT04875455已完成不适用

Development of a Database (Register) for Quality Assurance and Optimization of the Postoperative Results of Premium Intraocular Lenses

Beaver-Visitec International, Inc.8 个研究点 分布在 1 个国家目标入组 133 人开始时间: 2017年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
133
试验地点
8
主要终点
Monocular Best corrected distance visual acuity (5 m)

研究概览

简要总结

Short and long-term analysis of the refraction correction and optical image quality of modern premium intraocular lenses (IOLs) with the establishment of a database for quality assurance and optimization the computation constants of the lens power.

详细描述

Since the investigational lens, like conventional IOLs, is a posterior chamber lens which is widely implanted following cataract extraction, phacoemulsification is adopted. To assess the binocular vision, the investigational lens will be mono- or bilaterally implanted.

Clinically retro- and prospective, non-randomized, uncontrolled, open study at several centers: University Eye Clinic Heidelberg (leading center), Practice Center Ahaus in the Eye Clinic Ahaus, Breyer, Kaymak & Klabe Eye Surgery in Düsseldorf, nordBLICK Eye Center Kiel.

Main objectives:

  1. Functional results (refraction and visual acuity results) Secondary goals:
  2. Deviation target vs. achieved postoperative refraction (for constant optimization of the IOL calculation)
  3. Subjective patient satisfaction
  4. Visual quality (e.g. scattered light, contrast vision, spherical aberrations)
  5. Stability of the results achieved postoperatively

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
45 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Monocular Best corrected distance visual acuity (5 m)

时间窗: Postoperative Day 75-105 (3 months)

CDVA measured with ETDRS charts placed in 5m distance with best aided corrective glasses according to ISO 11979-7:2014.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (8)

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