跳至主要内容
临床试验/NCT01884805
NCT01884805终止不适用

Feasibility of Measurement of Optical Aberrations in Hyperopia by Using an Adaptive Optics Visual Simulator (AOVIS-I)

University Hospital, Toulouse1 个研究点 分布在 1 个国家目标入组 9 人开始时间: 2013年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
9
试验地点
1
主要终点
Measurement of optical aberrations

研究概览

简要总结

The primary purpose of the protocol is to evaluate the adaptive optics visual simulator to measure optical aberrations in hyperopic eyes.

The study hypotheses are the:

  • Ability to measure optical aberrations in hypermetropia.
  • Knowledge of optical aberrations of the eye hyperopic.
  • To adapt therapeutic management in optical aberrations measured.

详细描述

The procedure is guided by the custom made software and its graphical user interface. The interface has been designed to be user-friendly, being very similar to the software usually managed by the clinicians in their daily professional practice. The complete procedure in one patient takes less than 5 minutes and is completely non-invasive. The optical measurements only involve the use of low power infrared laser and the visual testing is as simple for the patients as watching television and making responses.

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
否

入选标准

  • •hyperopic patients
  • •to be able to understand an information and give a consent
  • •affiliated to medical insurance

排除标准

  • •pregnant women or nursing mothers
  • •ocular infection
  • •keratitis
  • •restless patients
  • •ocular surgery 90 days before inclusion

研究组 & 干预措施

Monocular Adaptive Optics Visual Simulator (AOVIS-I)

Other

干预措施: Monocular Adaptive Optics Visual Simulator (AOVIS-I) (Device)

结局指标

主要结局

Measurement of optical aberrations

时间窗: 1 day (Participants will be followed for the duration of ophtalmology consultation)

Feasibility of Measurement of optical aberrations in hyperopia by using an Adaptive Optics Visual Simulator AOVIS-I. Outcome measure is assessed during a consultation

次要结局

  • Reproductibility of the measures(1 day (Participants will be followed for the duration of ophtalmology consultation))
  • Quantitative measurement of optical aberrations(1 day (Participants will be followed for the duration of ophtalmology consultation))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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