跳至主要内容
临床试验/NCT01662778
NCT01662778已完成4 期

The Clinical Effect in Asthma of Inhaled Fluticasone Propionate Delivered as Monodisperse Aerosols

Imperial College London2 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2011年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
21
试验地点
2
主要终点
AMP Challenge Test PC20

研究概览

简要总结

The objective here is to determine that the efficiency of inhaled drug delivery can be improved by using a fine mist cloud of drug particles (as opposed to a coarse mist cloud of drug particles). This information will be valuable in designing new inhalers in order to improve their beneficial effects and reduce their side effects, by using the least possible drug dose to achieve a good patient response.

.

详细描述

Inhaled drug therapy is an established and effective means to treat lung diseases such as asthma. Medical inhalers ('puffers') form the cornerstone of the management of patients with respiratory/lung problems. Inhaled treatment usually comprises placing an inhaler (puffer) in the mouth and inhaling a measured dose of drug from the puffer. The drug dose needs to bypass the throat and reach the lungs, in order to be effective.

However, there is still much that is not known about what actually happens to the inhaled drug in the lungs. Much of the inhaled drug dose from a puffer fails to reach the lungs with most of it hitting the back of the throat. Only a small amount (approximately as little as 20%) of the drug reaches the important parts of the lungs to have a beneficial effect. Particle size has a significant influence on our ability to get the inhaled drug to the important parts of the lungs. In order to get the inhaled drug to these important parts of the lungs it is necessary to understand how much of a clinical improvement is obtained when identical doses of FP are inhaled with different particle sizes.

Inhalers (are a bit like hairspray cans or air fresher cans) and produce aerosol clouds of particles. Medical inhalers come in different shapes and sizes and have a variety of drugs used to treat patients. Inhalers used in routine clinical practice produce a 'coarse' mist of drug particles, which have the potential for side effects, as different sized particle will deposit in different parts of the respiratory tract and include; the mouth, the throat, the windpipe, and the bloodstream (all places we do not want the inhaled drug to 'deposit') and the lungs (where we do want the drug to go). This is particularly an important consideration with inhaled steroids that are commonly used in the management of patients with asthma and bronchitis and emphysema. For example, a common side effect is that the deposition of steroid drug in the throat can lead to a hoarse or altered voice, and sometimes thrush of the throat.

In contrast, monodisperse aerosols are special 'fine-mist' aerosols, where all the drug particles are of one particle size. We can use these aerosols to investigate the science of the way the lungs handle and respond to inhaled drugs of different particle size.

We shall use small and large drug particles. In order to deliver the inhaled drug as a monodisperse aerosol, we shall use a spinning top aerosol generator (STAG) (a large research nebuliser machine) which is able to selectively generate aerosol clouds that have a fine mist. This is an efficient machine compared to current nebulisers used in routine clinical practice, where it can often be difficult to control the inhaled drug dose to the patient; sometimes the patient gets too little a dose because the nebuliser is an inefficient inhaler device. But, also, by improving the efficiency of inhaled drug delivery - will allow lower drug doses to be used - which will decrease the potential for patient side effects.

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
Single (Participant)

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

  • Male or females aged greater than 18 years with a documented history of reversible airways disease responding to beta2-adrenergic therapy.
  • Asthmatic patients who are free from significant cardiac, gastrointestinal, hepatic, renal, haematological, neurological and psychiatric disease.
  • Patients who are stabilized on 500 micrograms or less of inhaled beclomethasone dipropionate or alternative inhaled corticosteroid (budesonide or ciclesonide).
  • Patients who are able and willing to give written informed consent to take part in the study
  • Not taking any regular medication that is contraindicated in those about to receive fluitcasone propionate (as indicated in the British National Formularly); other than the oral contraceptive pill.

排除标准

  • Those requiring maintenance oral or parenteral corticosteroid therapy for their airways disease or patients who have ceased maintenance oral or parenteral corticosteroid therapy within the four weeks prior to visit 1
  • Those requiring greater than 500 micrograms of inhaled beclomethasone dipropionate or alternative inhaled corticosteroid (budesonide or ciclesonide).
  • Subjects that have received inhaled or intravenous fluticasone propionate in the last 2 months.
  • Those whose reversible airways obstruction has been unstable in the last four weeks (indicated by any change in their maintenance therapy).
  • Those participants who have had a lower respiratory tract infection in the previous four weeks
  • Those who have donated 450ml blood or more within the previous 1 month.
  • Those who have a history of drug allergy which, in the opinion of the Unit Physician, contraindicates his/her participation in the study.
  • Any female volunteer or females who are pregnant or lactating or are likely to become pregnant during the trial. Women of child-bearing potential may be included in the study if, in the opinion of the investigator, they are taking adequate contraceptive precautions.
  • Participants with a known or suspected allergy to corticosteroids or any component of the formulations and/or Suspected hypersensitivity to inhaled corticosteroid (this will be asked directly at the screening visit).
  • Any patient with a contraindication to taking an inhaled steroid and specifically FP, listed in the British National Formulary will not be entered into this study
  • Those who have experienced an acute asthma exacerbation requiring emergency room treatment and/or hospitalisation within one month of visit 1.

研究组 & 干预措施

Monodisperse FP 1.5um

Active Comparator

50 mg of monodisperse Fluticasone Propionate delivered as 1.5 microns aerosol followed by AMP PC20 challenge test

干预措施: 1.5 microns at 50mg (Drug)

Monodisperse FP 6.0um

Active Comparator

50 mg of monodisperse Fluticasone Propionate delivered as 6.0 microns aerosol followed by AMP PC20 challenge test

干预措施: 6 microns at 50mg (Drug)

Placebo STAG

Placebo Comparator

No active drug, just solvent delivered from STAG followed by AMP PC20 challenge test

干预措施: Placebo Comparator (Drug)

MDI FP

Active Comparator

Fluticasone Propionate , Metered dose inhaler, 250 mg dose followed by AMP PC20 challenge test

干预措施: MDI FP (Drug)

结局指标

主要结局

AMP Challenge Test PC20

时间窗: 2 hours

The concentration of Adenosine Monophosphate (AMP), measured in mg/ml, required to see a 20% fall in the patient's forced expiratory volume in 1 second (FEV1) is measured after taking FP aerosol. AMP is a bronchoconstrictor agent (ie it narrows the airways. We would expect that more would be necessary to produce the same 20% fall in FEV1 after receiving the FP than before due to the reduction in airways inflammation. This change is the primary outcome measure.

次要结局

  • Multi-breath Nitrogen Washout Test(0 and 4 hours)
  • Spirometry(0 and 4 hours)
  • The Concentration of Fluticasone Propionate(4 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验