跳至主要内容
临床试验/TCTR20180903006
TCTR20180903006已完成不适用

Correlation between relative afferent pupillary defect (RAPD) and visual field defect on Humphrey automated perimetry

Prince of Songkla University0 个研究点目标入组 56 人开始时间: 2018年9月3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
56

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
20 Years 至 N/A (No limit)(—)
性别
All

入选标准

  • 1)The patients are diagnosed with unilateral or asymmetrical bilateral optic neuropathy or retinopathy
  • 2)The patients have RAPD using neutral density filters and swinging light test
  • 3)The patients are willing and able to provide informed consent to participate in the study
  • 4)The patients are at age above 20 years old

排除标准

  • 1)The patients have advance retinopathy or optic neuropathy
  • 2)The patients have pupil irregularity in the abnormal RAPD eye such as posterior synechiae, iris atrophy, post laser peripheral iridotomy or iridoplasty, iris sphincter tear, iridodialysis, neovascular iris, corectopia, and traumatic mydriasis.
  • 3)The patients use one of medications affecting the pupil size: dilating or constricting eye drops
  • 4)The patients have media opacities that obscure pupillary examination or have an effect on visual field analysis such as cataract, corneal opacity, and vitreous hemorrhage
  • 5)The patients are diagnosed with cranial nerve III palsy with pupillary involvement or Horners syndrome
  • 6)The patients cannot perform visual field test with Humphrey automated perimetry program 30-2, SITA-standard strategy
  • 7)The patients with unreliable Humphrey visual filed studies which define as one of these following:
  • I.False-negative errors greater than 30%
  • II.False-positive errors greater than 30%
  • III.Fixation loss greater than 20%

研究者

相似试验

Correlation between relative afferent pupillary... | 临床试验