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Inhaled Steroids and Control of Severe Asthma (INHALE)

2020年11月6日 更新者:Carmen Brittinger、University of Giessen

Inhaled Steroids and Control of Severe Asthma: Comparison of the AKITA Technology Versus Conventional MDI (INHALE)

Investigational device: AKITA 2 device versus conventional metered-dose inhaler (MDI)

Objectives: To explore if inhalative fluticasone application by means of the AKITA technology would result in a better symptom control in patients with severe persistent asthma as compared to inhalative application of fluticasone by a conventional MDI.

Study design: open label, cross-over (one AKITA, one MDI arm)

Patients: 20 Patients with severe persistent asthma

研究概览

地位

终止

研究类型

观察性的

注册 (实际的)

6

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Giessen、德国、35392
        • Justus-Liebig-University Giessen
      • Greifenstein、德国
        • Lungenfachklinik Waldhof Elgershausen
      • Marburg、德国
        • Philipps-Universitat Marburg

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

16年 至 78年 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

取样方法

概率样本

研究人群

Patients with severe persistent asthma

描述

Inclusion Criteria:

  • Severe persistent asthma bronchiale with diagnosis according to the criteria of the Global Initiative for Asthma (GINA) executive summary
  • Treatment with at least inhaled corticosteroids (ICS) and long acting b agonists (LABA)
  • Evidence of inflammatory triggered form of asthma with at least one of the following:
  • sensitization to typical aerogenous allergens
  • increased Serum IgE levels
  • Eosinophilia in peripheral blood
  • Proven Eosinophilia in sputum differential (> 3%) in the previous 2 years
  • at least 2 exacerbations of asthma within the previous 24 months leading to unscheduled presentation at a health care provider and/or systemic corticosteroid
  • Signed informed consent
  • Requirements of the local ethics committee are met

Exclusion Criteria:

  • Acute exacerbation of asthma within the last 6 weeks Rtot > 350% predicted capillary pO2 < 60mmHG, pCo2 > 50mmHG near fatal asthma or anaphylaxis in history
  • Age ≤ 18 and > 80 years
  • Active smoking or > 15 pack-years former smoking
  • Oral steroid treatment with a prednisolon-equivalent dose exceeding 10 mg per day
  • Pregnancy, nursing females
  • Female without use of effective contraceptive method
  • Treatment with investigational drugs over the past 30 days or during the course of the trial
  • Severe and uncontrolled gastroesophageal reflux disease
  • Ongoing psychiatric disorder
  • Treatment with systemic corticosteroids for any reason other than asthma
  • Other active lung diseases
  • Medical history of other uncontrolled diseases 3 months prior randomization (e.g. infections, coronary heart diseases and metabolic diseases)
  • Any history of malignancy requiring ongoing treatment and/or limiting life-expectancy
  • Clinically significant abnormalities in electrocardiogram (ECG) or laboratory exams
  • Asthma related to non-steroidal anti-inflammatory drug (NSAID)
  • Insulin dependent diabetes mellitus
  • Cataract

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 观测模型:病例对照
  • 时间观点:预期

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Asthma control
大体时间:38 weeks
Changes in asthma control, measured by Juniper Asthma Control Questionnaire during the 16 week treatment period in AKITA versus MDI based steroid application. Physician will assess level of asthma control in accordance with criteria from Gaining Optimal Asthma Control (GOAL) study.
38 weeks

次要结果测量

结果测量
措施说明
大体时间
Standardized asthma related quality of life questionnaire (AQLQs)
大体时间:38 weeks
AQLQs will be completed at screening, randomization, crossover and at end of study
38 weeks
Steroid, fluticasone and reliever medication use
大体时间:38 weeks
doses of systemic steroids and fluticasone dosage will be assessed and documented. Frequency of use of reliever medication will be summed from patient's diary and documented.
38 weeks
Lung function
大体时间:38 weeks
Pulmonary function tests (PFT) will be performed and lung function will be assessed by means of spirometry and body plethysmography.
38 weeks
Diffusing capacity for carbon monoxide
大体时间:38 weeks
Diffusing capacity for carbon monoxide will be assessed at rest and holding breath at full inspiration.
38 weeks
Capillary blood gas analysis
大体时间:38 weeks
Capillary blood gas analysis will be obtained from the arterialized ear lobe.
38 weeks
Measurement of Fractional Concentration of Nitric Oxide in Exhaled Air (feNO)
大体时间:38 weeks
feNO will be assessed at each visit. Measurements will be performed following the recommendations of the American Thoracic Society (ATS) and the European Respiratory Society (ERS).
38 weeks
Cell differential in induced sputa
大体时间:1 day
Induced sputum will be obtained at screening if not done within the previous 2 years.
1 day
Adrenal function
大体时间:38 weeks
Determination of the fraction of urinary cortisol has been used for screening of adrenal hypo- or hyperfunction and showed to be as effective as 24 hour urinary free cortisol excretion. Urine samples will be obtained at baseline, randomization, crossover and end of study.Values will be recorded.
38 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

合作者

调查人员

  • 首席研究员:Andreas Guenther, MD、University of Gießen

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2010年9月1日

初级完成 (实际的)

2018年12月28日

研究完成 (实际的)

2018年12月28日

研究注册日期

首次提交

2010年8月18日

首先提交符合 QC 标准的

2010年9月8日

首次发布 (估计)

2010年9月9日

研究记录更新

最后更新发布 (实际的)

2020年11月10日

上次提交的符合 QC 标准的更新

2020年11月6日

最后验证

2020年11月1日

更多信息

与本研究相关的术语

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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