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临床试验/PACTR202207762785564
PACTR202207762785564Other3 期

Evaluation of the Efficacy, safety, and tolerability of Difluprednate 0.05% versus Prednisolone acetate 1% eye drops following uneventful phacoemulsification surgery

Suez Canal University Hospital0 个研究点目标入组 800 人开始时间: 2022年7月4日最近更新:
适应症

试验速览

阶段
3 期
状态
Other
发起方
入组人数
800

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
45 Year(s) 至 64 Year(s)(—)
性别
All

入选标准

  • 1.Age more than 50 years
  • 2.Patients diagnosed to have cataract, LOCS III cataract classification: NO = 2 and NC = 2)

排除标准

  • 1.Known sensitivity to any of the ingredients in this study medication
  • 2.History of glaucoma or ocular hypertension in the study eye
  • 3.Previous history of steroid-induced increase of intraocular pressure (IOP)
  • 4.Previous ocular surgery
  • 5.history of uveitis
  • 6.Intraoperative complications as posterior capsule rupture
  • 7.Diabetic patients, Pregnancy, Autoimmune patients, and Single eyed patient.

研究者

发起方
Suez Canal University Hospital

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