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临床试验/CTRI/2021/11/038002
CTRI/2021/11/038002尚未招募未知

on-inferiority of Nanodropper-mediated microdrops vs. standard drops of 0.5% timolol maleate in patients with open-angle glaucoma or ocular hypertension - NIND

anodropper Inc0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方

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

  • 1. Patients with a recent diagnosis of primary open angle glaucoma (POAG) or ocular hypertension (OHT) and are not taking any ophthalmic medications for whom 0.5% timolol maleate would be prescribed as a first-line treatment
  • 2. Participants must have corrected Snellen visual acuity of 6/60 or better in each eye
  • 3. The baseline IOP should be between 21 and 35 mmHg as assessed by Goldmann applanation tonometry

排除标准

  • 1. A recent history (within the past 6 months) of ocular trauma, infection, or uveitis
  • 2. Baseline IOP of < 21 mmHg
  • 3. Baseline IOP of > 35 mmHg
  • 4. History of cardiovascular, pulmonary, cerebrovascular, or chronic renal disease
  • 5. History of borderline or uncontrolled systemic arterial hypertension
  • 6. Use of any systemic α-agonist or β-blocker within 30 days of study commencement
  • 7. History of receiving general anesthesia within the previous 30 days
  • 8. Pregnant women and nursing mothers

研究者

发起方
anodropper Inc

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