NCT01114581已完成2 期
Evaluating the Effect of Mucinex 1200mg on Mucociliary and Cough Clearance During an Acute Respiratory Infection
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
- 否
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
研究点 (1)
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