跳至主要内容
临床试验/NCT00333255
NCT00333255已完成3 期

Preoperative and Postoperative Nevanac 0.1% Compared to Acular LS for the Treatment of Ocular Inflammation Associated With Cataract Surgery

Alcon Research2 个研究点 分布在 1 个国家目标入组 267 人开始时间: 2005年9月最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
267
试验地点
2
主要终点
Percentage of patients who are a clinical success at Day 14 postoperative visit (where a "clinical success" is defined as aqueous cells < grade 1 and aqueous flare = grade 0 at the current visit and all subsequent visits).

研究概览

简要总结

The purpose of this study is to compare the effectiveness of Nepafenac Ophthalmic Suspension, 0.1% eye drops to Acular LS eye drops, used before and after cataract surgery, for treating inflammation in the eye.

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
Single

入排标准

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

入选标准

  • planned cataract extraction with posterior chamber intraocular lens implantation

排除标准

  • 未提供

结局指标

主要结局

Percentage of patients who are a clinical success at Day 14 postoperative visit (where a "clinical success" is defined as aqueous cells < grade 1 and aqueous flare = grade 0 at the current visit and all subsequent visits).

次要结局

  • Percentage of patients who are clinically cured, clinical successes, treatment failure, clinically significant inflammation

研究者

申办方类型
Industry

研究点 (2)

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