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临床试验/CTRI/2015/12/006473
CTRI/2015/12/006473Other2 期

SAFETY AND EFFICACY OF BRIMONIDINE TARTRATE OPHTHALMIC SUSPENSION 0.35%ONCEDAILY AND ALPHAGAN® P 0.1%THRICE DAILY IN PATIENTS WITH OPEN ANGLE GLAUCOMA OROCULAR HYPERTENSION: A RANDOMIZED, OPEN LABEL, PARALLEL GROUP, ACTIVECONTROLLED STUDY

Sun Pharma Advanced Research Company Limited0 个研究点目标入组 50 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
Other
入组人数
50

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

入选标准

  • Willing and able to give written informed consent.
  • -diagnosis of OHG or OAG
  • -Unmedicated IOP >= 22 mmHg and <= 36 mm Hg in one or
  • -Women of child bearing potential practicing an acceptable method of birth control

排除标准

  • -Women who are Pregnant nursing or planning a pregnancy or who were of childbearing potential and not using reliable method of contraception
  • -Known lack of ocular hypotensive response to topical ophthalmic alpha adrenergic receptor agonists in the opinion of the Investigator
  • -Severe or serious hypersensitivity to alpha-adrenergic agonist drugs
  • -Intraocular conventional surgery in any eye within the past six months

研究者

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