跳至主要内容
临床试验/NCT00452114
NCT00452114终止不适用

A Randomized, Controlled Study Evaluating the Effectiveness of the Inexsufflator Cough Assist Device in Patients With Symptomatic Bronchiectasis

University of Massachusetts, Worcester2 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2004年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
发起方
入组人数
28
试验地点
2
主要终点
Number of Suppurative Exacerbations Per Patient Per Year

研究概览

简要总结

This study is a randomized, controlled trial examining the effectiveness of the mechanical cough-assist device (in-exsufflator) in promoting the clearance of retained airway secretions in patients with symptomatic bronchiectasis. We hypothesize that this enhanced clearance of airway secretions will lead to a decline in the number of acute exacerbations of bronchiectasis experienced by these patients during the study period, improve health-related quality of life, decrease overall health-care costs and improve pulmonary function.

详细描述

Bronchiectasis is characterized by airway dilatation with the potential to cause devastating illness, including repeated respiratory infections requiring antibiotics, disabling productive, mucopurulent cough, shortness of breath and occasional hemoptysis. The damaged and dilated airways lead to persisting bacterial infection of the bronchi and bronchioles, causing inflammation and retained secretions, which in turn may further damage the airways. Patients typically suffer from frequent, severe and refractory episodes of bacterial bronchitis, often requiring hospitalization and prolonged courses of antibiotics. The pathophysiology of bronchiectasis involves the retention of viscid, tenacious inflammatory secretions and microbes leading to a "vicious cycle" of airway obstruction, destruction and recurrent infection with further compromise of the mucociliary clearance host defense apparatus. It has been widely proposed and recommended that methods of enhancing clearance of airway secretions should be an integral component of the care of patients with bronchiectasis. Despite these recommendations and a sound pathophysiologic plausibility given the central role retention of secretions plays in the disease, the effectiveness of interventions targeted toward enhancing bronchopulmonary hygiene has not been systematically studied. It is also not known whether the ability to generate an adequate cough would predict which patient will benefit from these interventions.

The mechanical in-exsufflator device assists patients in clearing retained secretions by augmenting the expiratory flow and force of the patient's cough with the addition of a cycle of positive and negative inspiratory pressure. An effective cough mechanism is actually an important and beneficial host defense which aids in mucus clearance along with the mucociliary apparatus. We hypothesize that daily, regular use of the in-exsufflator device will lead to a reduction in acute bronchiectasis exacerbations- a clinically meaningful endpoint- with other possible beneficial outcomes including improved pulmonary function, improved health-related quality of life and decreased health care costs.

Despite the lack of rigorous, well-designed studies supporting the role and most effective mode of bronchial hygiene physiotherapy in patients with bronchiectasis, many Pulmonologists recommend the flutter valve device as the generally accepted "standard of care" at this time due to its relative non-invasiveness, ease of use and high level of patient acceptability. The flutter valve is a simple, hand-held, pipe-like device which helps loosen secretions by providing an expiratory low-pressure vibratory pulse to the patient's airway when used. This study will provide a comparison of the clinical efficacy of these mechanical chest physiotherapy devices in the setting of bronchiectasis.

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
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
否

入选标准

  • •Chest CT scan confirmation of bronchiectasis
  • •At least two exacerbations in the preceding 12 months requiring antibiotics

排除标准

  • •Cystic fibrosis
  • •Bullous emphysema
  • •History of spontaneous pneumothorax
  • •History of massive hemoptysis: greater than 200 cc in a 24 hour period
  • •Lung resection surgery in the past 6 months
  • •Use of the mechanical cough in-exsufflator in the prior 3 months
  • •Inability to speak and read English
  • •Inability to demonstrate proper use of the cough-assist or flutter device
  • •Unable to provide informed consent

研究组 & 干预措施

Assignment to In-Exsufflator Cough Assist Device

Active Comparator

In-Exsufflator Cough Assist Device augments the expiratory flow and force of the patient's cough with the addition of a cycle of positive and negative inspiratory pressure when used daily

干预措施: In-Exsufflator Cough Assist Device (Device)

Assignment to flutter valve device

Active Comparator

flutter valve device delivers expiratory low-pressure vibratory pulse to the patient's airway when used daily

干预措施: Active Comparator: Flutter Valve Device (Device)

结局指标

主要结局

Number of Suppurative Exacerbations Per Patient Per Year

时间窗: 12 months

The impact of the intervention is measured by the total number of suppurative exacerbations per patient within a 12 month period.

Number of Hospitalizations and Urgent/Unscheduled Outpatient Visits

时间窗: 12 months

The impact of the intervention is measured by the number of hospitalizations and urgent/unscheduled outpatient visits the participants experienced within a 12 month period.

次要结局

  • Quality of Life (St. George's Respiratory Questionnaire)(12 months)
  • Quality of Life (Cough-Specific Quality of Life Questionnaire)(12 months)

研究者

发起方
University of Massachusetts, Worcester
申办方类型
Other
责任方
Principal Investigator
主要研究者

Stephen Krinzman

Principal Investigator

University of Massachusetts, Worcester

研究点 (2)

Loading locations...

相似试验

In-exsufflator Cough Assist Device in Patients With... | 临床试验