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临床试验/KCT0006770
KCT0006770尚未招募未知

A Prospective, Multicenter Comparative Case-Control Study to investigate the Clinical Efficacy of 0.1% Tacrolimus in Patients with Corneal Neovascularization

Korea University Ansan Hospital0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
20?(Year) 至 70?(Year)(—)
性别
All

入选标准

  • 1) Patients who visited Asan Medical Center, Yonsei University Severance Hospital, and Korea University Ansan Hospital, were diagnosed with corneal neovascularization and voluntarily agreed to participate in the clinical trial.
  • 2) Corneal neovascularization is diagnosed based on the following criteria.
  • i. When blood vessels and opacities are observed from the limbus to the center of the cornea

排除标准

  • 1) In case of active ocular surface inflammatory disease
  • 2) Those who have used Cyclosporine, steroids, or systemic immunosuppression (Glucocorticoids, Cyclophosphamide, Azathioprine, Methotrexate, etc.) within 2 weeks of the test period
  • 3) History of ophthalmic surgery and trauma within the last 3 months.
  • - However, if LASEK/LASIK has been operated within 12 months, it is not possible to participate in the clinical trial.
  • 4) Those who are planning ophthalmic surgery (including LASIK/LASIK) during the study period
  • 5) Pregnant women, lactating women, and female patients planning to become pregnant
  • 6) Patients with hypersensitivity to investigational drugs
  • 7) Patients who are allergic to fluorescein or eye drops
  • 8) Contact lens wearers
  • 9) Others judged inappropriate by the investigator

研究者

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