CTRI/2024/08/072298尚未招募4 期
Evaluation of Nanodropper-mediated Microdrops vs Conventional Dropsof Proparacaine HCL 0.5 Percentage - Nil
anodropper, Inc.0 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
- 4 期
- 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 = 18 years
- •2) Ability to provide informed consent for mode of topical anesthesia delivery
- •3) Ability to verbally respond to pain
- •4) Receiving treatment at AEH OPD (patient has undergone a preliminary examination and is awaiting dilation)
排除标准
- •1)Have a contraindication to local anaesthetics.
- •2)Intravitreal injection within the past 14 days.
- •3)Recent ocular surgery within the past 4 weeks.
- •4)Preexisting diagnosis of ocular surface disease. requiring punctal plug placement.
- •5)Evidence of any current ocular inflammation/infection.
- •6)Any previous ocular condition (i.e., neurotrophic keratitis, herpetic eye disease, presence of a corneal graft, etc.) that has permanently altered the native sensation of the ocular surface.
- •7)Use of contact lenses.
- •8)Use of exclusionary medications:
- •9)Topical steroid drops, NSAIDS, IOP lowering eye drops, any anti-viral medications used for herpes, Opioids
研究者
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