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临床试验/NCT03322111
NCT03322111Unknown不适用

Assessment of Cyclofusion Capabilities of Normal Subjects and Patients With 3D Dynamic Random-dot Stereograms

Cantonal Hospital of St. Gallen0 个研究点目标入组 50 人开始时间: 2018年1月最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
50
主要终点
In- and excyclofusion competence in healthy individuals. Change in In- and excyclofusion competence in patients who need a strabismus surgery before and 6 month after surgery.

研究概览

简要总结

With this study the investigator wants measure the individual cyclofusion competence from healthy subjects and patients suffering from Strabismus with a only binocularly visible threedimensional Landolt-C stimulus. For this the participant has to look at a 3-D monitor with shutter glasses. The participant is sitting in 2 meter distance in front of the monitor. On the monitor appears the Landolt-C stimulus as a dynamic Random-Dot Stimulus. As long as the participant can fuse the stimulus he will be able to see the Landolt C-ring threedimensional. The participant is then ask to tell in which direction the notch of the Landolt-C ring points out. Once a critical degree of cyclotorsion is reached the participant will no longer be able to see the Landolt C ring and the individual cyclofusion competence is reached.

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
12 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Visual acuity >0,4; Stereopsis

排除标准

  • Visual acuity <0,4; no Stereopsis

研究组 & 干预措施

Cyclofusion

Experimental

干预措施: measurement of the cyclofusion (Diagnostic Test)

结局指标

主要结局

In- and excyclofusion competence in healthy individuals. Change in In- and excyclofusion competence in patients who need a strabismus surgery before and 6 month after surgery.

时间窗: Once in healthy individuals. Before and 6 month after a (independent from the study) performed strabismus surgery.

The maximum in- and maximum excyclofusion competence will be measured with the described test set-up. The results will be documented in degree.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Prof. Dr. Veit Sturm

Prof. Dr.

Cantonal Hospital of St. Gallen

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