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临床试验/NCT01610804
NCT01610804已完成不适用

Choroidal Thickness Measurements During CSCR Treatment Applying EDI-OCT Technology

University Hospital Regensburg1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2011年4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
18
试验地点
1

研究概览

简要总结

The purpose of this study is to determine changes in choroidal thickness in patients with Central Serous Chorioretinopathy (CSCR) during the first 3 months after initial diagnosis via Enhanced-Depth-Imaging-Spectral-Domain-Optical-Coherence-Tomography (EDI-OCT).

Study hypothesis: Since exudative changes in the choroid seem to constitute the primary pathology of CSCR, changes in choroidal thickness compared to healthy eyes should be present and be visible using EDI-OCT.

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with initial diagnosis of CSCR and no treatment so far

排除标准

  • Therapy (drugs/laser) due to CSCR

研究者

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

Caroline Brandl

MD

University Hospital Regensburg

研究点 (1)

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