IRCT2016081629386N1已完成未知
Comparison of Loteprednol 0.5% with Fluorometholone 0.1% after Myopic Photorefractive Keratectomy (PRK)
Vice Chancellor Of Research, Shahid Beheshti University of Medical Sciences0 个研究点目标入组 62 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 62
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
- 年龄范围
- 18 years 至 50 years(—)
- 性别
- All
入选标准
- •age more than 18 years;
- •stable refraction for at least 12 month with myopia between -8.0 to -1.0 Diopters and astigmatism less than 4.0 Diopters;
- •normal eye examination (except refractive error);
- •corrected distance visual acuity (CDVA) of 20/20;
- •no history of systemic or autoimmune disease or receiving immunosuppressive treatment;
- •neither pregnant nor breast feeder;
- •using no topical ophthalmic medication;
- •have no contraindication for PRK.
- •Exclusion criteria:
- •Patients were unable to return for follow-up or needed to increase drug dosage for any reason;
- •patients who did not follow the instructions correctly;
- •patients with anisometropia (more than 1 diopter) or significant pre-operative central corneal thickness difference between two eyes (more than 20 µm); those who received MMC just in one eye;
- •patients with postoperative complications like keratitis.
排除标准
- 未提供
研究者
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