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
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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