跳至主要内容
临床试验/NCT00382681
NCT00382681已完成不适用

Clinical Evaluation of the Safety and Efficacy of an Investigational Multi-Purpose Disinfecting Solution Compared to a Marketed Multi-Purpose Solution for Care of Soft Contact Lenses

Alcon Research2 个研究点 分布在 1 个国家目标入组 252 人开始时间: 2004年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
252
试验地点
2
主要终点
Lens Cleanliness - Residual lens lysozyme (HPLC) at Day 90 on Group IV lenses

研究概览

简要总结

The objective of the study was to clinically evaluate the safety and effectiveness of a new multi-purpose disinfecting solution for soft contact lenses.

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

性别
All
接受健康志愿者

入选标准

  • Successful daily wear of FDA Group I or IV lenses on a two-week or longer replacement schedule for at least one month.
  • Use of a multi-purpose solution only as the pre-study care regimen for at least one month (rewetting drops use is also acceptable).
  • Successful lens wear for at least 8 hours per day.
  • Vision correctable to 20/
  • Normal eyes - no current ocular abnormalities that prevent successful contact lens wear.
  • No corneal surgery within the past 12 months.
  • No systemic disease that affects that eye or that could be worsened by the use of contact lenses or solutions.
  • No over-the-counter or prescription ocular medication.
  • No enrollment in another clinical study within 30 days prior to enrollment.

排除标准

  • 未提供

结局指标

主要结局

Lens Cleanliness - Residual lens lysozyme (HPLC) at Day 90 on Group IV lenses

时间窗: Day 90

次要结局

  • Average Lens Wearing Time(Day 90)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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