ACTRN12616001397404终止1 期
Intranasal Deposition of fluorescein-dyed Saline delivered by a Nasal Mesh Nebulizer (NMN) at different pulse frequencies in patients that have undergone Functional Endoscopic Sinus Surgery (FESS)
适应症
试验速览
- 阶段
- 1 期
- 状态
- 终止
- 入组人数
- 20
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •1. Participants (both males and females) that have undergone Functional Endoscopic Sinus Surgery (FESS) more than 3 months before the study
- •2. Age >= 18 years
- •3. No history of smoking
- •4. No history of chronic lung diseases including asthma, cystic fibrosis, tuberculosis, chronic obstructive lung disease
- •5. Normal lung function with stable and reproducible baseline FEV1 of >80% of predicted value following adjustment for height, age, and gender (according to the Global Lung Initiative equation)
排除标准
- •1. Significant upper and/or lower respiratory tract infection within the previous 4 weeks
- •2. History of recurrent lung infections
- •3. History of chronic lung diseases
- •4. History of severe or multiple allergies, including hay-fever and perennial rhinitis
- •5. Participants using nasal decongestant within 14 days of entering the study
- •6. Participants with documented or suspected, clinically significant alcohol or drug abuse
- •7. Known history of adverse reaction to fluorescein
研究者
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