跳至主要内容
临床试验/NCT01114581
NCT01114581已完成2 期

Evaluating the Effect of Mucinex 1200mg on Mucociliary and Cough Clearance During an Acute Respiratory Infection

Reckitt Benckiser LLC1 个研究点 分布在 1 个国家目标入组 38 人开始时间: 2010年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
38
试验地点
1
主要终点
Percent of Inhaled Radioactive Tracer Particles Cleared From Lungs

研究概览

简要总结

The purpose of this research study is to explore the mechanism of action of Mucinex, an oral, over-the-counter, FDA approved expectorant in patients with acute respiratory tract infections.

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
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Symptoms of cough, thickened mucus and chest congestion
  • Able to produce sputum
  • Non Smoker

排除标准

  • Fever above 101°F
  • Any chronic illness

研究组 & 干预措施

Guaifenesin

Active Comparator

Mucinex 1200mg (Guaifenesin)given as 2, 600mg tablets

干预措施: Mucinex (Drug)

Placebo

Placebo Comparator

Given as 2 tablets

干预措施: Placebo (Drug)

结局指标

主要结局

Percent of Inhaled Radioactive Tracer Particles Cleared From Lungs

时间窗: 3 hours following inhalation of radioactive tracer particles

Percentage of inhaled radioactive tracer (Ave180Clear)

次要结局

  • Guaifenesin AUC(0-3)(3 hours following dose administration)
  • Assess Sputum Properties (Objective Measures) and Symptoms (Subjective Measures) After Treatment With Mucinex or Placebo.(Within 10 days of developing symptoms associated with a respiratory tract infection)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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