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临床试验/JPRN-UMIN000005931
JPRN-UMIN000005931已完成未知

Clinical evaluation of 0.1% olopatadine hydrochloride ophthalmic solution in pediatric patients - Clinical evaluation of 0.1% olopatadine hydrochloride ophthalmic solution in pediatric patients

Alcon Japan Ltd.0 个研究点目标入组 40 人开始时间: 2011年7月5日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
40

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

年龄范围
7years-old 至 16years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1.Patients having ocular itching sensation and injection (caused by disease other than allergic conjunctivitis) possibly affecting the evaluation of drug efficacy 2.Patients having retinal detachment, diabetic retinopathy or progressive retinal disease (excluding cases rated by the attending physician as causing no problem in enrollment to the study) 3.Patients with a history of ocular infection (bacterial, viral or fungal), corneal herpes or relapsing corneal erosion of sudden onset or secondary to corneal injury (excluding cases rated by the attending physician as causing no problem in enrollment to the study) 4.Patients having received continuous treatment with corticosteroid (subconjunctival injection) within 3 months (90 days) before acquisition of consent 5.Patients having received immunotherapy (desensitization, immunomodulating therapy, etc.) 6.Patients requiring continuous treatment of corticosteroid, immunosuppressors, non-steroidal anti-inflammatory agents, vasoconstrictors, anti-histamines, anti-allergy agents, herb preparations indicated for "conjunctivitis" or any ophthalmic solution other than the test product 7.Patients having undergone ocular laser therapy within 3 months (90 days) before acquisition of consent or non-laser ocular surgery within 6 months (180 days) after acquisition of consent or planned to receive surgery during the study period 8.Unilaterally blind patients (best corrected visual acuity: below 0.01) 9.Patients with a history of allergy or hypersensitivity to olopatadine hydrochloride 10.Patients necessitating the use of contact lens during the study period 11.Other patients judged by the attending physician as inappropriate for the study

研究者

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