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临床试验/NCT00579189
NCT00579189已完成3 期

Safety and Efficacy of a Topical Otic Formulation in the Treatment of Acute Otitis Media With Otorrhea Through Tympanostomy Tubes (AOMT)

Alcon Research0 个研究点目标入组 776 人开始时间: 2006年1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
776
主要终点
Time to cessation of otorrhea as recorded by the parent or guardian via a patient diary

研究概览

简要总结

The purpose of this study is to determine if a topical otic formulation is safe and effective in treating middle ear infections in patients with ear tubes.

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
6 Months 至 12 Years(Child)
性别
All
接受健康志愿者

入选标准

  • 6 months to 12 years old
  • Ear tubes in one or both ears
  • Ear drainage visible by the parent / guardian
  • Ear drainage less than 21 days
  • Ear tube may not be silver oxide, silver salt, t-type tube or long-shafted tube
  • Patient may not have non-tube otorrhea
  • Patient may not have had otic surgery other than tube placement in the last year
  • Patient may not be a menarchal female
  • Diabetic patients are not eligible
  • Patient may not have any disease or condition that would negatively affect the conduct of the study
  • Patient may not require any other systemic antimicrobial therapy during the study.
  • Patient must meet certain medication washouts to be eligible
  • Analgesic use (other than acetaminophen) is not allowed
  • Patient may not be pre-disposed to neurosensory hearing loss
  • Other protocol-defined inclusion criteria may apply

排除标准

  • Other protocol-defined exclusion criteria may apply

研究组 & 干预措施

Moxidex

Experimental

Moxidex otic solution

干预措施: Moxidex otic solution (Drug)

Moxidex

Experimental

Moxidex otic solution

干预措施: Tympanostomy tubes (Device)

Moxifloxacin

Active Comparator

Moxifloxacin otic solution

干预措施: Moxifloxacin otic solution (Drug)

Moxifloxacin

Active Comparator

Moxifloxacin otic solution

干预措施: Tympanostomy tubes (Device)

结局指标

主要结局

Time to cessation of otorrhea as recorded by the parent or guardian via a patient diary

时间窗: From baseline

次要结局

  • Clinical cure rate(From baseline)
  • Microbiological outcome(From baseline)
  • Treatment failures(From baseline)

研究者

申办方类型
Industry
责任方
Sponsor

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