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临床试验/IRCT2016081629386N1
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

发起方
Vice Chancellor Of Research, Shahid Beheshti University of Medical Sciences

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