跳至主要内容
临床试验/CTRI/2023/06/053775
CTRI/2023/06/053775尚未招募Unknown

Dexamethasone against yellow sub-threshold micropulse laser in the treatment of chronic central serous chorioretinopathy (DAYA) - Nil

Hyderabad Eye Research Foundation0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
尚未招募

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1.Adults of both genders aged 30 years or more
  • 2.Diagnosis of cCSC confirmed at screening visit by complete ocular examination and multimodal imaging in the study eye
  • 3.Best corrected vision score of 73 to 19 at test distance of 4 meters on ETDRS chart at recruitment (Snellen equivalent 20/40 to 20/400)
  • 4.Decrease in vision primarily secondary to cCSC
  • 5.Willing to sign informed consent form before initiation of any study related procedure.

排除标准

  • 1.Patients not able to comply with the study or follow up procedures
  • 2.Laser/ PDT treatment for CSC within 3 months of enrolment
  • 3.Use of corticosteroids in all forms within 3 months of enrolment
  • 4.Pharmacological treatment (eplerenone) for CSC within a month of enrolment
  • 5.Eyes with choroidal neovascularization demonstrable on multimodal imaging (OCTA/FA/ICGA)
  • 6.Non-study eye vision of <20/200,
  • 7.Aphakia in study eye
  • 8.History of glaucoma in either eye (IOP >24 mmHg)
  • 9.Cataract grade dense enough to affect retinal imaging
  • 10.History of hypersensitivity to fluorescein dye
  • 11.Presence of sub-retinal fluid (SRF) or intra-retinal fluid (IRF) secondary to causes other than CSC
  • 12.Presence of active infectious disease or intra-ocular inflammation, active or suspected periocular infection in either eye at the time of enrolment
  • 13.History of intra-ocular surgery within 3 months in the study eye prior to the randomization
  • 14.Pregnancy induced CSC.

研究者

相似试验

A randomized double blinded sham-controlled study to... | 临床试验