跳至主要内容
临床试验/NCT00705159
NCT00705159已完成4 期

Safety and Efficacy of Zylet vs Lotemax, Tobramycin and Vehicle in Pediatric Blepharoconjunctivitis

Bausch & Lomb Incorporated1 个研究点 分布在 1 个国家目标入组 137 人开始时间: 2008年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
137
试验地点
1
主要终点
Change From Baseline in the Total Blepharoconjunctivitis Grade.

研究概览

简要总结

The objective of this study is to evaluate the safety and effectiveness of Zylet in comparison with Lotemax, Tobramycin and the vehicle of Zylet for the treatment of blepharoconjunctivitis in pediatric subjects.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
1 Week 至 6 Years(Child)
性别
All
接受健康志愿者

入选标准

  • children 0-6 years of age.
  • clinical diagnosis of blepharoconjunctivitis
  • Parent/guardian must understand, be willing and able to comply with all treatment and follow-up procedures.
  • Parent/guardian must understand, be willing and able to provide informed consent and Health Insurance Portability Accountability Act (HIPAA) authorization.

排除标准

  • Known hypersensitivity to corticosteroids, aminoglycosides, or any component of the study medication.
  • Subjects who have a history of ocular surgery, including laser procedures, within the past 6 months.
  • Subjects who are monocular.
  • Subjects who have a history of any severe/serious ocular pathology or medical condition that could result in the subject's inability to complete the study.
  • Subjects who have participated in an ophthalmic drug or device research study within 30 days prior to entry in this study.

研究组 & 干预措施

Loteprednol etabonate and tobramycin

Experimental

Drug: Zylet (loteprednol etabonate and tobramycin)

干预措施: loteprednol etabonate and tobramycin (Drug)

Loteprednol etabonate

Active Comparator

Drug: Lotemax (loteprednol etabonate)

干预措施: loteprednol etabonate (Drug)

Tobramycin

Active Comparator

Drug: Tobramycin

干预措施: Tobramycin (Drug)

Vehicle

Placebo Comparator

Vehicle of Zylet

干预措施: Vehicle of Zylet (Drug)

结局指标

主要结局

Change From Baseline in the Total Blepharoconjunctivitis Grade.

时间窗: Baseline to 15 days

Change from baseline to visit 4 in the total blepharoconjunctivitis grade. Graded on a scale of 0-4, 0 (none), 1 (minimal/trace), 2 (mild), 3 (moderate), and 4 (severe). Grade range from 0-32.

次要结局

  • Change From Baseline in Total Blepharoconjunctivitis Graded at Visit 2(Baseline to Day 3)
  • Change From Baseline in Total Blepharoconjunctivitis Graded at Visit 3(Baseline to Day 7)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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