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临床试验/NCT04769453
NCT04769453终止不适用

Multicenter Ab-interno Glaucoma Study Investigating Canaloplasty, Randomized, Controlled Trial: iTrack (Nova Eye Medical) Compared to Omni (Sight Sciences)

Nova Eye, Inc.14 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2021年4月29日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
20
试验地点
14
主要终点
Reduction in mean Intraocular pressure (IOP) and glaucoma medication use at 12 months post-intervention

研究概览

简要总结

A prospective, multicenter, randomized, single-masked clinical trial to evaluate the effectiveness outcomes of canaloplasty performed as a standalone procedure with the iTrack microcatheter to the Omni surgical system, and to compare the effectiveness of two types of Ophthalmic Viscoelastic Device (OVD).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
22 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed with mild to moderate open angle Glaucoma.
  • Visual Field test (Humphrey SITA standard 24-2) with mean deviation better than or equal to -12.0 dB
  • IOP < or = to 36 mmHG while on one to four ocular hypotensive medications
  • Shaffer grade of > or = III in all four quadrants
  • Able and willing to comply with the Protocol and follow up visits for 12 months

排除标准

  • Laser trabeculoplasty other than selective laser trabeculoplasty (SLT)
  • History of iStent or iStent inject within 180 days of the screening visit
  • History of ECP or Micropulse laser
  • Trabeculectomy or other bleb forming procedure including Xen, Express and glaucoma drainage device/valves
  • Prior canaloplasty (ab interno and ab externo)
  • Prior goniotomy or trabeculotomy
  • History of Hydrus microstent or suprachoroidal stent
  • History of cataract surgery within 6 months of screening
  • Acute angle closure, traumatic, congenital, malignant, uveitic or neovascular glaucoma, pigmentary or pseudoexfoliative glaucoma

结局指标

主要结局

Reduction in mean Intraocular pressure (IOP) and glaucoma medication use at 12 months post-intervention

时间窗: 12 months

IOP will be measured at each study visit using Goldmann applanation tonometry

次要结局

  • Complications intra-operatively and post-operatively associated with the iTrack canaloplasty microcatheter compared to complications intra-operatively and post-operatively with the OMNI surgical system.(12 months)
  • Visual acuity at 12 months compared to baseline visual acuity(12 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (14)

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