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临床试验/NCT02555995
NCT02555995已完成不适用

Assessment of Scan Quality of Sparse OCT Retina Scanner (MimoStudy01)

University of Bern2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2015年11月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
2
主要终点
Distance between ILM and RPE (IPD) measurement successful or not. Successful is defined as a) measurement performed/failed, and if performed, b) value obtained within ±10% of value of reference OCT device.

研究概览

简要总结

Optical Coherence Tomography (OCT) is an established non-invasive medical imaging technique ophthalmologists use to diagnose and monitor retinal diseases such as age-related macular degeneration (AMD).

This study assesses the scanning performance of a newly developed sparse OCT retina scanner that is smaller and more compact than most commercially available medical OCT systems. The prototype device was developed at Artorg Center Bern and Berner Fachhochschule Biel.

In this study the device is first tested on human eyes. The scanning performance is compared to a reference device. Additionally patient feedback during the examination is acquired.

The findings of this study are used to improve the software and the ergonomics of the investigational device.

详细描述

Background

Optical Coherence Tomography (OCT) is an established non-invasive medical imaging technique ophthalmologists use to diagnose and monitor retinal diseases such as age-related macular degeneration (AMD).

This study assesses the scanning performance of a newly developed sparse OCT retina scanner that is smaller and more compact than most commercially available medical OCT systems. The prototype device was developed at Artorg Center Bern and Berner Fachhochschule Biel.

In this study the device is first tested on human eyes. The scanning performance is compared to a reference device. Additionally patient feedback during the examination is acquired.

The findings of this study are used to improve the software and the ergonomics of the investigational device.

研究设计

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

入排标准

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

入选标准

  • 18 years or older
  • German speaking
  • Suffering from age-related macular degeneration
  • Written informed consent
  • Exclusion Criteria
  • Parkinsonian syndrome
  • Pregnant women
  • Persons using electronic medical aids i.e. hearing aid, pacemaker..

排除标准

  • 未提供

结局指标

主要结局

Distance between ILM and RPE (IPD) measurement successful or not. Successful is defined as a) measurement performed/failed, and if performed, b) value obtained within ±10% of value of reference OCT device.

时间窗: During diagnostic intervention, expected to be ca. 30 minutes on average

次要结局

  • Patient comfort during examination(Directly after diagnostic intervention, expected to be ca. 35 minutes on average)
  • Duration of OCT examination with investigational device(Directly after diagnostic intervention, expected to be ca. 35 minutes on average)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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