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临床试验/NCT01105949
NCT01105949已完成1 期

An Evaluation of Two Novel Breathe Right Nasal Strip Prototypes on Nasal Patency

GlaxoSmithKline1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2009年9月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
50
试验地点
1
主要终点
Change from baseline in minimum cross sectional area (second restriction) of the nasal valve using acoustic rhinometry

研究概览

简要总结

The results of this study will help in the development of a new type of nasal strip for management of nasal congestion and snoring.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • •Good general health with (in the opinion of the investigator) no clinically significant and relevant abnormalities of medical history

排除标准

  • •Currently experiencing cold or flu
  • •History of perennial or allergic rhinitis or rhinitis medicamentosa
  • •Evidence of nasal polyps as documented by anterior rhinoscopy
  • •Evidence of significant nasal tract structural malformations including a severe deviated septum (where subjects are indicated for surgery) or a concha bullosa as documented by anterior rhinoscopy
  • •Visible open sores, sunburn, irritation, eczema or chronic skin condition on the face to nose
  • •Bacterial sinusitis infection during 2 weeks prior to entry in the baseline phase of the study
  • •Any other condition that in the opinion of the investigator would have an affect on nasal breathing
  • •Use of any product containing menthol within two hours prior to any subjective measures involved in the study
  • •Had an allergic contact dermatitis on the face within 30 days prior to entry
  • •History of chronic or active skin or other immunologic (rheumatoid, psoriasis) disease
  • •History of skin cancer
  • •Use of antibiotics or alpha adrenergic drugs (all forms) within 1 week prior to entry in the baseine phase of the study
  • •Use of glucocorticosteroids (all forms) within 1 month prior to entry in the baseline phase of the study
  • •Any current treatment which in the opinion of the investigator will affect nasal congestion

研究组 & 干预措施

NexGen AB 2R11

Experimental

NexGen AB 2R11

干预措施: NexGen AB 2R11 (Device)

Marketed nasal strip

Other

Marketed nasal strip

干预措施: Marketed nasal strip (Device)

NexGen JB Organic PET/PE

Experimental

NexGen JB Organic PET/PE, prototype nasal dilator strip

干预措施: NexGen JB Organic PET/PE (Device)

结局指标

主要结局

Change from baseline in minimum cross sectional area (second restriction) of the nasal valve using acoustic rhinometry

时间窗: baseline to within 2 hours post application

Change from baseline in total nasal volume of the nose using acoustic rhinometry

时间窗: baseline to within 2 hours post application

次要结局

  • Nasal airway breathing as measured by Posterior Rhinomanometry(Baseline to 2 hours)
  • Nasal airway breathing as measured by Peak Nasal Inspiratory Flow (PNIF)(Baseline to 2 hours)
  • Subjective perceptions of airway breathing(Baseline to 2 hours)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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