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临床试验/NCT00770133
NCT00770133已完成3 期

A Multi-center, Double-masked, Randomized, Placebo-controlled Evaluation of the Onset and Duration of Action of KetoNaph Ophthalmic Solution in the Conjunctival Allergen Challenge (CAC) Model of Acute Allergic Conjunctivitis.

Bausch & Lomb Incorporated1 个研究点 分布在 1 个国家目标入组 141 人开始时间: 2010年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
141
试验地点
1
主要终点
Ocular Itching

研究概览

简要总结

The purpose of this study is to establish the safety and efficacy of ketotifen/naphazoline ophthalmic solution compared to vehicle and its individual components in alleviating the signs and symptoms of conjunctival allergen challenge (CAC)-induced allergic conjunctivitis.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

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

入选标准

  • Positive history of ocular allergies and positive skin test reaction to cat hair, cat dander, grasses, ragweed, and/or trees within the past 24 months.
  • Calculated best-corrected visual acuity of 0.7 logMAR or better in each eye as measured using the ETDRS chart.
  • Positive bilateral conjunctival allergen challenge(CAC) reaction within 10 minutes of instillation of the last titration of allergen at visit
  • Positive bilateral CAC reaction for at least 2 out of 3 time points at visit 2.

排除标准

  • Known contraindications or sensitivities to the study medication or its components.
  • Any ocular condition that, in the opinion of the investigator, could affect the subjects safety or trial parameters.
  • Use of disallowed medications during the period indicated prior to study enrollment or during the study.

研究组 & 干预措施

Ketotifen/naphazoline

Experimental

Ketotifen/naphazoline ophthalmic solution administered in either the right eye, left eye or both eyes at visit 3 and visit 4.

干预措施: Ketotifen/naphazoline (Drug)

Vehicle

Placebo Comparator

Vehicle of ketotifen/naphazoline ophthalmic solution administered in either the right eye, left eye or both eyes at visit 3 and visit 4.

干预措施: Vehicle (Drug)

Naphazoline

Active Comparator

Naphazoline ophthalmic solution administered in either the right eye, left eye or both eyes at visit 3 and visit 4.

干预措施: Naphazoline (Drug)

Ketotifen

Active Comparator

Ketotifen ophthalmic solution administered in either the right eye, left eye or both eyes at visit 3 and visit 4.

干预措施: Ketotifen (Drug)

结局指标

主要结局

Ocular Itching

时间窗: 3, 5, and 7 minutes post challenge at 14 days

Ocular itching was evaluated by the participant at 3, 5, and 7 minutes post challenge. Assessments were made using a 0-4 numerical analog scale, allowing 0.5-unit increments (but disallowing 0.25-unit increments), where: 0.0=None and 4.0=Incapacitating itch with an irresistible urge to rub

Conjunctival Redness

时间窗: 7, 15, and 20 minutes post challenge at 14 days

Conjunctival hyperemia was evaluated by the Investigator at 7, 15, and 20 minutes post challenge. Assessments were completed using a 0-4 numerical analog scale, allowing 0.5-unit increments, where: 0.0=None and 4.0=Extremely severe.

次要结局

  • Episcleral Redness(7, 15, and 20 minutes post challenge at 14 days)
  • Chemosis(7, 15, and 20 minutes post challenge at 14 days)
  • Eyelid Swelling(7, 15, and 20 minutes post challenge at 14 days)
  • Percentage of Eyes With Ocular Mucus Discharge(7, 15, and 20 minutes post challenge at 14 days)
  • Ciliary Redness(7, 15, and 20 minutes post challenge at 14 days)
  • Percentage of Eyes With hTearing(7, 15, and 20 minutes post challenge at 14 days)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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