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临床试验/NCT03751631
NCT03751631已完成3 期

A Double-Masked, Active-Controlled Study of the Safety and Efficacy of Phenylephrine 2.5%-Tropicamide 1% Ophthalmic Solution Administered With a Microdose Dispenser for Dilation of the Pupil

Eyenovia Inc.1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2018年11月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
Eyenovia Inc.
入组人数
70
试验地点
1
主要终点
Change in Pupil Diameter From Baseline

研究概览

简要总结

This study evaluated pupil dilation after administration of fixed combination tropicamide-phenylephrine (TR/PE) vs. phenylephrine (PE) alone and tropicamide (TR) alone. Participants attended 3 visits. At each visit, after baseline measurements, 1 of the 3 drugs was administered to both eyes, then pupil dilation and safety assessments were performed at specific time intervals.

详细描述

Volunteer participants were screened for study eligibility during a Screening Visit and enrolled after signing the study-specific informed consent form. Subjects meeting all inclusion/exclusion criteria were scheduled for 3 treatment visits, which were at least 2 days, but no more than 7 days apart. At each treatment visit, baseline measurements were taken, then 1 of the 3 study drugs was administered to both eyes (each participant's drug administration sequence was randomly determined). Afterwards, efficacy and safety assessments were performed at 20, 35, 50, 65, 80, 120, and 180 minutes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Diagnostic
盲法
Double (Participant, Outcomes Assessor)

盲法说明

There were no differences in the presentation of drug administered and all study personnel conducting ophthalmic assessments after drug administration were masked to treatment assignment.

入排标准

性别
All
接受健康志愿者

入选标准

  • Ability to provide written consent and return for all study visits
  • Photopic pupil diameter <= 3.5 mm in each eye

排除标准

  • Allergy to phenylephrine hydrochloride, tropicamide, or benzalkonium chloride
  • History of benign prostatic hyperplasia
  • Use of a benzodiazepine, monoamine oxidase inhibitor, tricyclic antidepressant, anticonvulsant, or cholinergic drug
  • History of closed-angle glaucoma
  • Anatomically narrow anterior chamber angles
  • Ocular surgery or laser treatment of any kind
  • History of chronic or acute uveitis
  • History of traumatic iritis or hyphema
  • History of traumatic mydriasis or angle recession
  • History of heterochromia
  • Irregularly-shaped pupil secondary to ocular trauma or congenital defect.
  • History of neurogenic pupil disorder
  • History of anterior chamber intraocular lens (IOL) or iris-fixated IOL
  • History of iris surgery, iris atrophy, or iris-cornea apposition/touch
  • Unwilling or unable to discontinue use of contact lenses at treatment visits.
  • Current active eye disease for which topical or systemic ophthalmic medication is necessary, except for dry eye disease managed using artificial tears.
  • Presence of a severe/serious ocular condition, or any other unstable medical condition that, in the Investigator's opinion, may preclude study treatment and/or follow-up
  • Pregnancy or lactation

研究组 & 干预措施

1-TR/PE, 2-TR, 3-PE

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Tropicamide 1%-Phenylephrine 2.5% ophthalmic solution (TR/PE) (Drug)

1-TR/PE, 2-TR, 3-PE

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Tropicamide 1% ophthalmic solution (TR) (Drug)

1-TR/PE, 2-TR, 3-PE

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Phenylephrine 2.5% ophthalmic solution (PE) (Drug)

1-TR/PE, 2-PE, 3-TR

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Tropicamide 1%-Phenylephrine 2.5% ophthalmic solution (TR/PE) (Drug)

1-TR/PE, 2-PE, 3-TR

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Tropicamide 1% ophthalmic solution (TR) (Drug)

1-TR/PE, 2-PE, 3-TR

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Phenylephrine 2.5% ophthalmic solution (PE) (Drug)

1-TR, 2-TR/PE, 3-PE

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Tropicamide 1%-Phenylephrine 2.5% ophthalmic solution (TR/PE) (Drug)

1-TR, 2-TR/PE, 3-PE

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Tropicamide 1% ophthalmic solution (TR) (Drug)

1-TR, 2-TR/PE, 3-PE

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Phenylephrine 2.5% ophthalmic solution (PE) (Drug)

1-TR, 2-PE, 3-TR/PE

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Tropicamide 1%-Phenylephrine 2.5% ophthalmic solution (TR/PE) (Drug)

1-TR, 2-PE, 3-TR/PE

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Tropicamide 1% ophthalmic solution (TR) (Drug)

1-TR, 2-PE, 3-TR/PE

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Phenylephrine 2.5% ophthalmic solution (PE) (Drug)

1-PE, 2-TR/PE, 3-TR

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Tropicamide 1%-Phenylephrine 2.5% ophthalmic solution (TR/PE) (Drug)

1-PE, 2-TR/PE, 3-TR

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Tropicamide 1% ophthalmic solution (TR) (Drug)

1-PE, 2-TR/PE, 3-TR

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Phenylephrine 2.5% ophthalmic solution (PE) (Drug)

1-PE, 2-TR, 3-TR/PE

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Tropicamide 1%-Phenylephrine 2.5% ophthalmic solution (TR/PE) (Drug)

1-PE, 2-TR, 3-TR/PE

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Tropicamide 1% ophthalmic solution (TR) (Drug)

1-PE, 2-TR, 3-TR/PE

Other

Participants were dosed once at 3 separate clinic visits in accordance with this sequence. Each participant received 2 sprays of the study drug in each eye.

干预措施: Phenylephrine 2.5% ophthalmic solution (PE) (Drug)

结局指标

主要结局

Change in Pupil Diameter From Baseline

时间窗: 35 minutes after initial dose

Difference in 35-minute pupil diameter vs. baseline measured using pupillometry in highly photopic conditions. Pupil diameter is reported in millimeters. For the change in pupil diameter, larger measurements indicate a better outcome.

次要结局

未报告次要终点

研究者

发起方
Eyenovia Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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